| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1039661197 |
| P356 | DOI | 10.1007/BF00284432 |
| P698 | PubMed publication ID | 184030 |
| P50 | author | Malcolm Ferguson-Smith | Q15436161 |
| P2093 | author name string | Ferguson-Smith MA | |
| Turleau C | |||
| de Grouchy J | |||
| Aitken DA | |||
| P2860 | cites work | Evidence for the assignment of the loci AK1, AK3and ACONsto chromosome 9 in man | Q28265339 |
| Linkage of the loci for the nail-patella syndrome and adenylate kinase | Q35231970 | ||
| A second family with the nail-patella allele and the adenylate kinase allele in coupling | Q35232399 | ||
| Localization of the human lactate dehydrogenase B gene on the short arm of chromosome 12 | Q35570053 | ||
| Evaluation of a possible sex difference in recombination for the ABO-AK linkage | Q35570897 | ||
| Data on the incidence, segregation and linkage relations of the adenylate kinase (AK) polymorphism | Q36567510 | ||
| Gene dosage: evidence for assignment of erythrocyte acid phosphatase locus to chromosome 2 | Q37460776 | ||
| Letter: Localisation of human gene for galactose-1-phosphate-uridyltransferase | Q39333456 | ||
| Letter: Superoxide dismutase in Down syndrome | Q39333517 | ||
| Probable assignment of the locus determining human red cell acid phosphatase ACP1 to chromosome 2 using somatic cell hybrids | Q43651068 | ||
| Partial trisomy 9q: a new syndrome | Q52113795 | ||
| Assignment by Deletion of Human Red Cell Acid Phosphatase Gene Locus to the Short Arm of Chromosome 2 | Q53804248 | ||
| Genetically Determined Variation of Adenylate Kinase in Man | Q59091962 | ||
| Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father | Q66879725 | ||
| Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11) | Q66879734 | ||
| Partial deletion of the short arm of chromosome 12(p11; p13). Report of a case | Q66879741 | ||
| Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1 | Q67432394 | ||
| [Increase of erythrocyte superoxide dismutase activity in trisomy for chromosome 21] | Q68350940 | ||
| GALACTOSAEMIA LOCUS AND THE DOWN'S SYNDROME CHROMOSOME | Q76535200 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 35-43 | |
| P577 | publication date | 1976-09-01 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34. | |
| P478 | volume | 34 |
| Q57195380 | A novel α-N-acetylgalactosaminidase family with an NAD+-dependent catalytic mechanism suitable for enzymatic removal of blood group A antigens |
| Q47283220 | ABO blood type/Rh factor and the incidence and outcomes for patients with triple-negative breast cancer |
| Q40323919 | Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature |
| Q33646081 | Association between ABO and Rh Blood Groups and Risk of Preeclampsia: A Case-Control Study from Iran |
| Q36359074 | Association of ABO and Colton Blood Group Gene Polymorphisms With Hematological Traits Variation. |
| Q40508093 | Banl RFLP atAK1locus (9q34) |
| Q40098239 | Biochemistry and Genetics of the ABO, Lewis, and P Blood Group Systems |
| Q40904698 | Blood group antigens: molecules seeking a function? |
| Q72021205 | Characterization of a complex Philadelphia translocation (1p-;9q+;22q-) by gene mapping |
| Q44561363 | Chromosome variation and gene action |
| Q24633042 | Comparison of nonerythroid alpha-spectrin genes reveals strict homology among diverse species |
| Q67701054 | Conversion of the human blood group H antigen to A antigenin vitro |
| Q40968148 | Detection of histo-blood group ABO mRNA in human chronic myeloid leukemia cell lines using reverse transcription-polymerase chain reaction (RT-PCR). |
| Q30959347 | Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man. |
| Q60361667 | EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9 |
| Q39862479 | Foot deformities associated with onycho-osteodysplasia. A familial study and a review of associated features |
| Q33681944 | Genetic counselling in hereditary osteo-onychodysplasia (HOOD, nail-patella syndrome) with nephropathy |
| Q48011202 | Heterogeneity of the blood group Ax allele: genetic recombination of common alleles can result in the Ax phenotype. |
| Q34163378 | Human delta-aminolevulinate dehydratase: chromosomal localization to 9q34 by in situ hybridization |
| Q36464270 | Is There an Association between Keloids and Blood Groups? |
| Q33675831 | Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-abl |
| Q35054247 | Mapping of human chromosomal regions related to neoplasia: Evidence from chromosomes 1 and 17 |
| Q34577589 | Mendelian Inheritance in Man and its online version, OMIM |
| Q36985969 | Modifying the red cell surface: towards an ABO-universal blood supply. |
| Q40665764 | Molecular genetics of ABO histo-blood groups |
| Q67560108 | Molecular genetics of hereditary nephritis |
| Q44272111 | Mouse chromosome 2. |
| Q71980308 | PK3: a new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalance |
| Q40349677 | Palmar-plantar hyperhidrosis occurring in a kindred with nail-patella syndrome. |
| Q34448661 | Regional assignment of the loci for adenylate kinase to 9q32 and for alpha 1-acid glycoprotein to 9q31-q32. A locus for Goltz syndrome in region 9q32-qter? |
| Q35203447 | Regional localization of human gene loci on chromosome 9: studies of somatic cell hybrids containing human translocations |
| Q40133201 | Segregation of ABO, AK1and ACONSin families with abnormalities of chromosome 9 |
| Q35198871 | Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9. |
| Q71168536 | Somatic cell genetics and gene mapping |
| Q70275221 | Suggested assignment of peptidase S (PEPS) to 4q11-4q12 by exclusion using gene dosage, accounting for variability in fibroblasts |
| Q48773764 | Unravelling the biochemical basis of blood group ABO and Lewis antigenic specificity |
| Q39020909 | Xeroderma pigmentosum in Egypt. III. ABO blood grouping in 22 affected families |
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