| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | C. B. Kerr | |
| P2860 | cites work | congenital disorder | Q727096 |
| Christmas disease: a condition previously mistaken for haemophilia | Q24569533 | ||
| Gene action in the X-chromosome of the mouse (Mus musculus L.) | Q29618263 | ||
| Stuart clotting defect. I. Segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, proconvertin, factor VII) deficiency | Q30448556 | ||
| Hemostatic data in relatives of hemophiliacs A and B; evidence for modifying the classical sex-linked recessive hypothesis | Q30838507 | ||
| Hemorrhagic diathesis associated with hyperheparinemia | Q78637366 | ||
| The role of Hageman factor in the initiation of blood coagulation | Q78641919 | ||
| [A case of congenital afibrinogenemia] | Q78664432 | ||
| V. Willebrand's disease and its treatment with a specific plasma fraction | Q78715932 | ||
| [Case of congenital afibrinemia.] | Q78740336 | ||
| [Use of a photometric test for the study of the effect of ADP on blood platelets.] | Q79694671 | ||
| [Phase contrast microscopy of the coagulocyte, coagulation islets and the coagulation of plasma in the blood of insects] | Q80749553 | ||
| The mutation rate of the gene for haemophilia, and its segregation ratios in males and females | Q83229412 | ||
| Coagulation studies | Q83451677 | ||
| Oral Contraception and Blood Coagulability | Q84947642 | ||
| Le facteur X | Q94137556 | ||
| [Congenital afibrinogenemia] | Q94273397 | ||
| Coagulation Studies in a Case of Hageman Trait | Q113854678 | ||
| Antihaemophilic factor deficiency, capillary defect of von Willebrand type, and idiopathic thrombocytopenia occurring in one family | Q33353473 | ||
| THE DUKE AND IVY METHODS FOR DETERMINATION OF THE BLEEDING TIME | Q33354358 | ||
| Hereditary pseudohaemophilia | Q33870709 | ||
| Sex Linkage in Man. | Q33946165 | ||
| A study of a case of congenital hypoprothrombinaemia | Q34250044 | ||
| WATERFALL SEQUENCE FOR INTRINSIC BLOOD CLOTTING. | Q34257361 | ||
| Observations on the hereditary nature of Hageman trait. | Q34648814 | ||
| Congenital afibrinogenemia; report on a child without fibrinogen and review of the literature | Q35229918 | ||
| Pseudohemophilia: report of 13 new cases and statistical review of previously reported cases | Q35234450 | ||
| Biosynthetic determination with radioactive sulfur of turn-over rates of various plasma proteins in normal and cirrhotic man | Q35303455 | ||
| Circulating anticoagulants: a study of 40 cases and a review of the literature. | Q35323162 | ||
| Hageman factor deficiency (Hageman trait). Case report and review of the literature | Q35352680 | ||
| Acquired hemophilia due to a circulating anticoagulant. Report of two cases, with review of the literature | Q35372557 | ||
| Review of the present status of other clotting factors: b) Factor VII (proconvertin). | Q35386287 | ||
| CHEMISTRY AND PHYSIOLOGY OF THE FIBRINOGEN-FIBRIN TRANSITION. | Q35442552 | ||
| CONGENITAL DEFICIENCY OF FACTOR VII (HYPOCONVERTINEMIA). CRITICAL REVIEW OF LITERATURE AND REPORT OF THREE CASES, WITH EXTENSIVE PEDIGREE STUDY AND EFFECT OF TRANSFUSIONS. | Q35450798 | ||
| A laboratory study of the carrier state in classic hemophilia | Q35561906 | ||
| A female case of haemophilia | Q35797581 | ||
| Congenital hypofibrinogenemia in five members of a family | Q35895424 | ||
| Sporadic cases of hemophilia and the question of a possible sex difference in mutation rates | Q35912230 | ||
| Linkage of color blindness to hemophilias A and B. | Q35912273 | ||
| Genetic Considerations in Familial Hemorrhagic Disease. I. The Sex-Linked Recessive Disorders, Hemophilia and PTC Deficiency | Q35912550 | ||
| Fibrinogen deficiency as a factor in haemorrhagic disease | Q36005782 | ||
| Familial haemophilia and factor VII deficiency | Q36702457 | ||
| Hemophilia (AHG deficiency) and factor VII (stable factor) deficiency in the American Indian. Report of four cases | Q38529020 | ||
| HEMOPHILIA. II. SOME PROPERTIES OF A SUBSTANCE OBTAINED FROM NORMAL HUMAN PLASMA EFFECTIVE IN ACCELERATING THE COAGULATION OF HEMOPHILIC BLOOD. | Q40924295 | ||
| Hemophilia A and concurrent factor VII deficiency. Studies of a patient with complicating cardiac tamponade | Q40994293 | ||
| The isolation and purification of a bovine-plasma protein which is a substrate for the coagulant fraction of Russell's-viper venom | Q42283834 | ||
| Possible implications of the autosomal and X-linked hemophilia phenotypes | Q43802329 | ||
| Vascular hemophilia: the association of a vascular defect with a deficiency of antihemophilic globulin | Q45866113 | ||
| Hemophilia A in a two year old girl | Q45866118 | ||
| Plasma thromboplastin antecedent (PTA) deficiency | Q45866262 | ||
| The correction of a hemorrhagic diathesis in preparation for surgery; the correction of plasma thromboplastin antecedent deficiency | Q45866286 | ||
| Assay of antihaemophilic globulin in treatment of haemophilic patients | Q45866298 | ||
| Deficiency of antihaemophilic globulin in heterozygous haemophilic females | Q45866346 | ||
| The antihaemophilic-globulin concentration in the plasma of female carriers of haemophilia | Q45866362 | ||
| Antihemophilic factor deficiency in the female. | Q45866449 | ||
| Observations on hemophilia, parahemophilia, and coexistent hemophilia and parahemophilia; alterations in the platelets and the thromboplastin generation test. | Q45866557 | ||
| Plasma antihaemophilic factor (AHF) concentrations in families of patients with haemorrhagic states | Q45866691 | ||
| Further evidence of resistance to warfarin in the rat. | Q54720365 | ||
| A mildly affected female haemophiliac. | Q55340709 | ||
| A CASE OF HAEMOPHILIA WITH MARFAN'S SYNDROME. | Q55396401 | ||
| combined deficiency of factor V and factor VIII | Q56014104 | ||
| A NEW ESTIMATE OF THE LINKAGE BETWEEN THE GENES FOR COLOUR-BLINDNESS AND HAEMOPHILIA IN MAN | Q56094410 | ||
| The Linkage between the Genes for Colour-Blindness and Haemophilia in Man | Q56094415 | ||
| The rate of spontaneous mutation of a human gene | Q56094417 | ||
| Die Chemie der Blutgerinnung | Q56169071 | ||
| BLEEDING AND COAGULATION IN SOME BERMUDAN CRUSTACEA | Q56175847 | ||
| Influence of Temperature upon Blood Coagulation in a Cold- and a Warm-blooded Animal | Q58958219 | ||
| A Tissue Fibrin-stabilizing Factor and Fibrinolytic Inhibition | Q58964882 | ||
| Gene Expression in Heterozygotes | Q59001834 | ||
| Ratio Adenosine Triphosphate/Adenosine Diphosphate in Platelet-rich Plasma in Hæmorrhagic Disorders (Von Willebrand and Glanzmann Disease) | Q59019694 | ||
| Synthesis of Plasma Antihæmophilic Factor | Q59023972 | ||
| Purification and Stabilization of Factor V | Q59027698 | ||
| Amino-Acid Sequence Investigations of Fibrinopeptides from Various Mammals: Evolutionary Implications | Q59054159 | ||
| A hitherto undescribed congenital haemorrhagic diathesis probably due to fibrin stabilizing factor deficiency | Q59461794 | ||
| Application of paper electrophoresis to separation of blood-clotting factors | Q64054670 | ||
| Congenital afibrinogenemia; report of a case | Q73107521 | ||
| Studies on the metabolism of fibrinogen in two patients with congenital afibrinogenemia | Q73196730 | ||
| Certain physical properties of bovine prothrombin | Q73205518 | ||
| Congenital familial deficiency of the stable prothrombin conversion factor; restudy of case originally reported as idiopathic hypoprothrombinemia | Q73206312 | ||
| [Observations on a case of essential fibrinogenopathy] | Q73212352 | ||
| [A rare hemorrhagic syndrome: afibrinogenemia: clinical presentation of a case] | Q73382957 | ||
| Congenital hypoproconvertinemia | Q73413205 | ||
| [Congenital afibrinogenemia; report of a case with multiple bone cysts and formation of a specific antibody (anti fibrinogen) following blood transfusion] | Q73425388 | ||
| [Genetic characteristics of Willebrand's disease from a new familial case] | Q73547849 | ||
| Congenital afibrinogenemia; a study of some basic aspects of coagulation | Q73581346 | ||
| [Congenital and familial afibrinogenemia; three cases] | Q73594503 | ||
| Blood clotting time and tissue mast cell number of the bat (Myotis lucifugus) in different physiological states | Q73594805 | ||
| Familial factor V deficiency: the pattern of heredity | Q73595246 | ||
| [Congenital afibrinogenemia; case report and review of literature] | Q73601447 | ||
| [Semeio-pathogenesis and classification of thrombopathic and hemophiliac hemorrhagic diathesis] | Q73626372 | ||
| Congenital hypoprothrombinemic states | Q73676393 | ||
| [Case of fibrinogen deficiency in the blood in child] | Q73695481 | ||
| Parahemophilia | Q73705666 | ||
| [Congenital factor V deficiency (parahemophilia) with true hemophilia in two brothers] | Q73712381 | ||
| [A case of total afibrinogenemia] | Q73926682 | ||
| [Two cases of familial hypoconvertinemia] | Q73942597 | ||
| Parahemophilia in three siblings (Owren's disease) | Q73979193 | ||
| [Tonsillectomy and hemorrhagic diathesis] | Q73982927 | ||
| Pseudohemophilia type B; hereditary hemorrhagic diathesis characterized by prolonged bleeding time and decrease in antihemophilic factor | Q73998822 | ||
| Congenital familial deficiency of factor V (parahaemophilia) combined with deficiency of antihaemophilic globulin | Q74141227 | ||
| A new coagulation defect | Q74141245 | ||
| Congenital hypoproconvertinemia | Q74318580 | ||
| Hemorrhagic diathesis due to factor VII deficiency | Q74370568 | ||
| Primary hemorrhagic diseases | Q74392617 | ||
| Christmas disease in a woman | Q74447535 | ||
| Congenital afibrinogenemia; report on a newborn infant without fibrinogen | Q74458082 | ||
| A case of congenital afibrinogenemia | Q74485715 | ||
| Congenital afibrinogenemia; the first case from Japan | Q74515419 | ||
| [Classic hemophilia in women] | Q74607928 | ||
| The blood groups of the western Walsers | Q74626253 | ||
| [Fibrin-stabilizing factor from thrombocytes] | Q74714571 | ||
| Studies on the polymerization of fibrin; the role of the globulin: fibrin-stabilizing factor | Q74785420 | ||
| Congenital coagulation deficiency of Stuart factor activity | Q74821606 | ||
| Haemolytic anaemia during treatment of leprosy with diaminodiphenylsulphone by mouth | Q75607799 | ||
| The influence of certain drugs on blood coagulation and related phenomena | Q75836307 | ||
| Transfusion Studies in von Willebrand's Disease: Effect on Bleeding Time and Factor VIII | Q76468348 | ||
| ELEVATION OF FACTOR VIII (ANTIHEMOPHILIC FACTOR) DURING PREGNANCY IN NORMAL PERSONS AND IN A PATIENT WITH VON WILLEBRAND'S DISEASE | Q76553584 | ||
| CONGENITAL AFIBRINOGENEMIA | Q76559372 | ||
| HEREDITARY DEFICIENCIES OF CLOTTING FACTORS VII AND X ASSOCIATED WITH CAROTID-BODY TUMORS | Q76560063 | ||
| FURTHER STUDIES ON CLOTTING AND FIBRINOLYSIS IN PLASMA FROM THE SMOOTH DOGFISH (MUSTELIS CANIS) | Q76595745 | ||
| ON THE PROPERTIES OF A NEW HUMAN FIBRINOPEPTIDE | Q76639117 | ||
| MILD HEMOPHILIA | Q76649289 | ||
| A NEW TEST FOR THE DETERMINATION OF THE FIBRIN STABILIZING FACTOR (FSF) | Q76656071 | ||
| BLOOD COAGULATION AND ANTICOAGULANT MECHANISMS IN THE TURTLE PSEUDEMYS ELEGANS | Q76700443 | ||
| COMBINED AHG- AND PTA-DEFICIENCY | Q76703597 | ||
| PLATELET CLUMPING IN VITRO | Q76708695 | ||
| THE STABILITY OF ANTIHEMOPHILIC GLOBULIN AND LABILE FACTOR IN HUMAN BLOOD | Q76713539 | ||
| CONGENITAL FACTOR V DEFICIENCY. A CLINICAL AND EXPERIMENTAL STUDY WITH REFERENCE TO PREVIOUSLY PUBLISHED CASES OF PARAHEMOPHILIA | Q76775497 | ||
| [STUDY OF NORMAL BLOOD COAGULATION IN TWINS WITH THE THROMBELASTOGRAPHIC METHOD.] | Q76782887 | ||
| FRUCTOSE-1 PHOSPHATE ALDOLASE DEFICIENCY IN TAY-SACHS DISEASE | Q76799549 | ||
| PLASMA FIBRIN STABILIZING FACTOR ACTIVITY IN VARIOUS DISEASES | Q76799880 | ||
| CONGENITAL DEFICIENCY OF THE FIBRIN STABILIZING FACTOR (FACTOR XIII). STUDY OF 2 CASES | Q76816725 | ||
| VITAMIN K INDUCED PROTHROMBIN FORMATION: ANTAGONISM BY ACTINOMYCIN D | Q76848688 | ||
| AN ASSAY FOR ANTIHAEMOPHILIC FACTOR (FACTOR VIII) WITH SOME CONSIDERATIONS AFFECTING THE ESTABLISHMENT OF A STANDARD REFERENCE PREPARATION | Q76878109 | ||
| THROMBASTHENIA. STUDIES ON THREE CASES | Q76878131 | ||
| ON A SWEDISH FAMILY WITH 51 MEMBERS AFFECTED BY VON WILLEBRAND'S DISEASE | Q76882155 | ||
| LOW IN-VIVO ADHESIVE-PLATELET COUNT IN HEREDITARY HAEMORRHAGIC TELANGIECTASIA | Q76922841 | ||
| A CLINICAL AND FAMILY STUDY OF HEREDITARY PROCONVERTIN (FACTOR VII) DEFICIENCY | Q76947317 | ||
| CLINICAL ASPECTS OF CONGENITAL FACTOR VII DEFICIENCY | Q76947320 | ||
| THE ROLE OF ENDOTOXIN IN THE EXTRACELLULAR COAGULATION OF LIMULUS BLOOD | Q76956779 | ||
| THE PLATELET FUNCTION OF THE THROMBOPATHY ON THE ALAND ISLANDS | Q76997062 | ||
| HAGEMAN FACTOR AND IN VIVO ACTIVATION OF FIBRINOLYSIS | Q77001211 | ||
| [ON THE PATHOGENESIS OF THE VON WILLEBRAND-JUERGENS SYNDROME. A CLINICAL AND SUBMICROSCOPICAL STUDY] | Q77072180 | ||
| TRANSFUSION THERAPY IN FACTOR 13 (F.S.F.) DEFICIENCY | Q77079610 | ||
| [Hemophiliacs of Tenna and their descendants, 1650-1955.] | Q77110113 | ||
| [Comparative determination of the antihemophilic globulin in both sexes] | Q77153642 | ||
| FAMILIAL GLANZMANN'S THROMBASTHENIA | Q77170241 | ||
| Afibrinogenaemia: case report of a child with recurrent bleeding. | Q54400587 | ||
| HEREDITARY TRANSMISSION OF EXCEPTIONAL RESISTANCE TO COUMARIN ANTICOAGULANT DRUGS. THE FIRST REPORTED KINDRED. | Q54714431 | ||
| CANINE HEMOPHILIA | Q77201666 | ||
| [Hemarthrosis due to proconvertin deficiency] | Q78229975 | ||
| The routine bleeding and clotting time tests: their medicolegal status | Q78285156 | ||
| Electrophoretic studies of the Prower factor; a blood coagulation factor which differs from factor VII | Q78317417 | ||
| A new approach to the thrombocytopathies; thrombocytopathy A | Q78404567 | ||
| The inadequacies of routine bleeding and clotting times | Q78436009 | ||
| [Hemophilia in the female; example of a clinical case of mild hemohemophilia in the mother of a patient with classic hemophilia.] | Q78475263 | ||
| [Hereditary factors in congenital deficiency of factor VII.] | Q78475682 | ||
| Congenital absence of fibrinogen: a rare cause of oral bleeding | Q78525902 | ||
| [Blood protein disorders in childhood.] | Q78593141 | ||
| [Study of the carriers of hemophillia] | Q78767014 | ||
| Congenital factor VII deficiency with normal Stuart activity: clinical, genetic and experimental observations | Q78809984 | ||
| Two typical hereditary charts of congenital factor VII deficiency | Q78821652 | ||
| [A new hemophilic tribe with von Willebrand-Juergen's disease (hereditary thrombopathy) from Aland (Finland).] | Q78831148 | ||
| Congenital deficiency of proconvertin: a clinical and laboratory report | Q78837952 | ||
| Hereditary labile factor (factor V) deficiency | Q78841625 | ||
| Precipitating antifibrinogen antibody appearing after fibrinogen infusions in a patient with congenital afibrinogenemia | Q78912067 | ||
| Acquired factor X deficiency in a patient with amyloidosis | Q78963053 | ||
| Combined deficiencies of PTA and AHG with vascular fragility | Q78968883 | ||
| Glanzmann's disease. Clinical, biological and pathogenic study apropos of 5 cases | Q78976848 | ||
| The Stuart-Prower factor: utilization of clotting factors obtained by starch-block electrophoresis for genetic evaluation | Q78983366 | ||
| Fibrinase III. Some enzymatic properties | Q78988622 | ||
| Von Willebrand’s Disease | Q79031877 | ||
| Further studies on the inheritance of Hageman trait | Q79059976 | ||
| Some experiences with a simplified micromethod for coagulation studies | Q79067638 | ||
| [On a case of Christmas disease associated with factor VII deficiency.] | Q79136417 | ||
| Clotting of echinoderm coelomic fluid | Q79167520 | ||
| [Study of a case of true congenital hypoproconvertinemia.] | Q79181393 | ||
| Clinical and laboratory studies of plasma thromboplastin antecedent deficiency (PTA) | Q79187838 | ||
| [Congenital and familial Stuart factor deficiency. Apropos of 2 personal cases considered congenital hypoconvertinemia.] | Q79191769 | ||
| [Hemophilia in a young girl] | Q79274044 | ||
| Plasmoptysis and gelation of erythrocytes in coagulation of blood of freshwater bony fishes | Q79304479 | ||
| Normal fibrinolytic system in blood in congenital afibrinogenemia and its significance | Q79337681 | ||
| The influence of fibrin stabilizing factor on the growth of fibroblasts in vitro and wound healing | Q79344271 | ||
| [Deficiency of the plasmatic antecedent of thromboplastin (PTA): description of new cases.] | Q79373142 | ||
| [On 4 cases of hemophilia A with partial deficiency of antihemophilic globulin.] | Q79377517 | ||
| Antihemophilic A factor (factor VIII) and fibrinogen in human blood. A study on the question of a closer correlation between the levels of the two factors | Q79381719 | ||
| Thrombo-embolism in patients with total proconvertin (factor VII) deficency. A report on two cases | Q79397553 | ||
| [A new familial coagulation disorder due to a deficiency of a fibrinstabilizing factor.] | Q79418105 | ||
| An antihaemophilic globulin (factor VIII) inhibitor: purification, characterization and reaction kinetics | Q79440668 | ||
| [3 cases of congenital afibrinogenemia in siblings. Genetic study.] | Q79446497 | ||
| [Clinical and biological observation of 3 cases of congenital afibrinogenemia in siblings.] | Q79446498 | ||
| [Congenital afibrinogenemia. Biological study of 2 cases.] | Q79452491 | ||
| [Congenital fibrinopenia. Comments onhe evolution of a case followed for 20 years.] | Q79460742 | ||
| Christmas factor: dosage compensation and the production of blood coagulation factor IX | Q79477468 | ||
| [Studies on a case of congenital afibrinogenemia. (On the role of blood coagulation in hemostasis)] | Q79504263 | ||
| [Congenital afibrinogenemia.] | Q79506503 | ||
| Acquired factor X deficiency associated with systematized amyloidosis--a report of a case | Q79526503 | ||
| [Apropos of 2 brothers suffering from congenital afibrinogenemia.] | Q79561478 | ||
| Congenital afibrinogenemia (a case report) | Q79565583 | ||
| Blood coagulation studies in hedgehogs, in a hibernating and a non-hibernating state, and in dogs, hypothermic and normothermic | Q79581988 | ||
| The treatment of haemorrhage in von Willebrand's disease and the blood level of factor VIII (AHG) | Q79593555 | ||
| von Willebrand's disease | Q79595846 | ||
| The importance of activation of antihemophilic globulin and proaccelerin by traces of thrombin in the generation of intrinsic prothrombinase activity | Q79601035 | ||
| Pathways to blood coagulation product I formation | Q79620986 | ||
| ??? | Q94221708 | ||
| ??? | Q94225181 | ||
| ??? | Q94229024 | ||
| ??? | Q94238212 | ||
| ??? | Q94256845 | ||
| ??? | Q94281497 | ||
| Haemophilia A in a girl. A probable exception from sex-linked recessive inheritance. | Q45866788 | ||
| A case of Hageman-factor deficiency and a method to purify the factor. | Q45866828 | ||
| Canine haemophilia B (Christmas disease). | Q45866844 | ||
| The mode of inheritance of PTA deficiency: evidence for the existence of major PTA deficiency and minor PTA deficiency. | Q45866884 | ||
| A chromosomal female with hemophilia A. | Q45866925 | ||
| Canine hemophilia. | Q45866959 | ||
| A method for the study of antihaemophilic globulin inhibitors with reference to six cases | Q45866988 | ||
| Fatal case of congenital plasma thromboplastin component deficiency: failure of response to therapy in Christmas disease | Q45867014 | ||
| "Mild hemophilia" affecting both males and females | Q45867130 | ||
| Classical hemophilia in a Filipino. | Q45867152 | ||
| Haemophilia in New Guinea. | Q45867158 | ||
| The carrier state in hemophilia A. | Q45867204 | ||
| The inheritance of Christmas factor | Q45867245 | ||
| Hemophilia B associated with a decreased factor VII activity. | Q45867280 | ||
| Equine haemophilia: report of a case and its response to multiple infusions of heterospecific AHG. | Q45867326 | ||
| Occurrence of two hemorrhagic disorders with antihemophilic factor (AHF) deficiency in the same family: classical hemophilia and von willebrand's disease | Q45867341 | ||
| Haemophilia syndromes. A survey of 267 patients | Q45867450 | ||
| The elderly haemophiliac | Q45867484 | ||
| TONSILLECTOMY IN PATIENTS WITH COAGULATION DEFECTS | Q45867496 | ||
| HAGEMAN FACTOR DEFICIENCY IN A CHILD | Q45867501 | ||
| HAEMOPHILIA DUE TO COMBINED DEFICIENCY OF AHG, PTC AND PTA FACTORS. | Q45867661 | ||
| HAEMOPHILIA IN THE DOG: TREATMENT WITH HETEROLOGOUS ANTI-HAEMOPHILIC GLOBULIN. | Q45867687 | ||
| HAEMOPHILIA, CHRISTMAS DISEASE AND THE XG BLOOD GROUPS. OBSERVATIONS BASED ON THE HAEMOPHILIACS OF BIRMINGHAM. | Q45867705 | ||
| ANTIHEMOPHILIC FACTOR IN CROSS-CIRCULATED NORMAL AND HEMOPHILIC DOGS. | Q45867711 | ||
| ABNORMAL BLOOD COAGULATION IN CARRIERS OF HEMOPHILIA | Q45867814 | ||
| STUDIES OF THE ANTIHEMOPHILIC FACTOR (AHF, FACTOR VIII) PRODUCED IN VON WILLEBRAND'S DISEASE. | Q45867823 | ||
| HEMOPHILIA--PATHOPHYSIOLOGIC STUDIES AND THE EVOLUTION OF TRANSFUSION THERAPY. | Q45867853 | ||
| ACTIVATION OF HAGEMAN FACTOR BY SOLUTIONS OF ELLAGIC ACID | Q45867870 | ||
| COAGULATION FACTORS IN NORMAL AND HEMOPHILIAC-TYPE SWINE. | Q45867876 | ||
| ANTIHEMOPHILIC GLOBULIN DEFICIENCY IN A CHROMOSOMAL FEMALE | Q45867900 | ||
| COMBINED HEMOPHILIA AND CHRISTMAS DISEASE | Q45868069 | ||
| ANTIHEMOPHILIC FACTOR LEVELS IN BLEEDER SWINE FOLLOWING INFUSIONS OF PLASMA AND SERUM. | Q45868228 | ||
| Combined hemophilia and PTC deficiency | Q45868477 | ||
| Variable manifestations of plasma thromboplastin component deficiency | Q45868524 | ||
| Haemophilia A in a "girl" with male sex-chromatin pattern | Q45868593 | ||
| Congenital vascular defect associated with platelet abnormality and antihemophilic factor deficiency | Q45868630 | ||
| Haemophilia in Sweden. I. Coagulation studies | Q45868730 | ||
| Haemophilia in Sweden. IV. Hereditary investigations | Q45868765 | ||
| A study of fibrinogen turnover in classical hemophilia and congenital afibrinogenemia | Q45868786 | ||
| Assay of plasma antihemophilic activity in normal heterozygous (hemophilia) and prothrombinopenic dogs | Q45872458 | ||
| Plasma thromboplastin component (PTC) deficiency; a new disease resembling hemophilia | Q45872591 | ||
| Hemophilia in twins | Q45878283 | ||
| OWREN'S DISEASES (CONGENITAL FACTOR V DEFICIENCY, PARAHEMOPHILIA) IN TWO NEGRO SISTERS | Q46257094 | ||
| Severe congenital hypoprothrombinemia in a Negro boy. | Q46576109 | ||
| PURIFICATION AND PROPERTIES OF BOVINE FACTOR V: A CHANGE OF MOLECULAR SIZE DURING BLOOD COAGULATION. | Q47422013 | ||
| Blood coagulation in fish | Q47746929 | ||
| A familial disorder of blood coagulation due to deficiency of the labile factor. | Q51047158 | ||
| Congenital afibrinogenemia. | Q51055727 | ||
| Familial congenital labile factor deficiency with syndactylism; investigation on the mode of action of the labile factor. | Q51058989 | ||
| Severe hypoprothrombinemia following propylthiouracil treatment of thyrotoxicosis. | Q51059171 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | blood coagulation | Q179217 |
| genetics | Q7162 | ||
| P304 | page(s) | 254-303 | |
| P577 | publication date | 1965-12-01 | |
| P1433 | published in | Journal of Medical Genetics | Q14640281 |
| P1476 | title | Genetics of human blood coagulation | |
| P478 | volume | 2 |
| Q70448317 | A report of a case of congenital afibrinogenemia |
| Q53765635 | Combined Deficiency of Factor V and Factor VIII: Report of a Family and Genetic Analysis |
| Q45856466 | Congenital combined factor V and factor VIII deficiency in a male born from a brother-sister incest |
| Q34283513 | Congenital dysprothrombinemia: an inherited structural disorder of human prothrombin |
| Q69593810 | Congenital factor VII deficiency. A case report |
| Q70968864 | Demonstration of a double hereditary pattern for congenital afibrinogenemia |
| Q69388973 | Hemorrhagic varicella in parahemophilia |
| Q35860499 | Heredity in Hæmatology |
| Q93694681 | Plasma factor-VIII concentrations in XXX women |
| Q42429855 | The genetic basis of variation in factor 8 levels among haemophiliacs |
| Q45858332 | The social impact of haemophilia |
| Q35569193 | Variations in levels of blood clotting factors IX and X in a population of normal men: possible genetic polymorphisms |
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