| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF00278725 |
| P698 | PubMed publication ID | 738728 |
| P2093 | author name string | B. Dutrillaux | |
| J. Lejeune | |||
| M. Prieur | |||
| A. Aurias | |||
| P2860 | cites work | Partial 7q trisomy due to t(7;12) (q22;q24) familial translocation | Q69103588 |
| [Partial trisomy 11q identified by study, with heat controlled denaturation, of the paternal balanced translocation] | Q69104986 | ||
| Familial balanced translocation t(2; 13) (q32; q33) and partial trisomy 2q | Q69125735 | ||
| [Translocation 46,XX, t(15; 21) (q13; q22,1) in the mother of 2 children with partial trisomy 15 and monosomy 21] | Q69125761 | ||
| [Trisomy 9p gy t(4; 9) (q 34; q21) mat] | Q69148552 | ||
| Identification of 2 familial translocations | Q69148593 | ||
| [Giemsa-R-banding analysis of the trisomy 9p and report of a new case] | Q69998822 | ||
| [New system of chromosome banding: the T bands (author's transl)] | Q70002573 | ||
| [Chromatid exchanges in human mitotic cells. BUDR Treatment and bichromatic fluorescence by aridine orange (author's transl)] | Q70029649 | ||
| [X-chromosome translocations. Examination based on treatment with BUDR and staining with acridine orange] | Q70030342 | ||
| Chromosomal Abnormalities in the Human Population: Estimation of Rates Based on New Haven Newborn Study | Q71447563 | ||
| [The role of parental translocations in cases of repeated miscarriages] | Q80252406 | ||
| An analysis of the break points of structural rearrangements in man | Q33585946 | ||
| The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature | Q33586909 | ||
| A cytogenetic survey of 11,680 newborn infants | Q34697792 | ||
| Mental retardation associated with "balanced" chromosome rearrangements | Q35202031 | ||
| AUTOSOMAL DISORDERS | Q35402353 | ||
| Location of Ribosomal DNA in the Human Chromosome Complement | Q37500615 | ||
| Various banding simultaneously obtained on the same slides, after treatment by BrdU (author's transl) | Q39371447 | ||
| Identification withGandRBanding of the Position of Breakage Points Induced in Human Chromosomes byin VitroX-irradiation | Q39391461 | ||
| Sequence of DNA replication in 277 R- and Q-bands of human chromosomes using a BrdU treatment | Q39411395 | ||
| Localization of chromatid breaks in Fanconi's anemia, using three consecutive stains | Q39444734 | ||
| Partial trisomy of chromosome 21 by maternal translocation t(15;21) (q26.2; q21) | Q39791289 | ||
| Partial 4q trisomy. Apropos of 3 cases | Q40329943 | ||
| Genetics of the +p9 syndrome | Q40498333 | ||
| Chromosome 8 : complete trisomy and segmental trisomies | Q40656670 | ||
| A theoretical model of structural chromosome rearrangement induction | Q40673247 | ||
| The Prader-Willi syndrome and 15-15 translocation | Q40673327 | ||
| Localization of γ-rays induced chromatid breaks using a three consecutive staining-technique | Q40850736 | ||
| Monosomy for the centromeric regions of chromosome 21 | Q43643747 | ||
| Analysis of a t translocation (18p+;21q-) by mild denaturation | Q43819458 | ||
| Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters | Q44289590 | ||
| 2 cases of trisomy 11q(q231--qter) by translocation t(11;22) (q231;q111) in 2 different families | Q44314659 | ||
| 2 cases of trisomy 11q(q23.2-- qter) with the same abnormality of external genitalia | Q44764097 | ||
| [Descriptive diagrams of human chromosomes (R band analysis and nomenclature according to the conference in Paris in 1971)] | Q50726228 | ||
| 47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22 | Q52110447 | ||
| Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 cases | Q52110748 | ||
| Incidence of chromosome aberrations among 11 148 newborn children | Q52113681 | ||
| Correlation between euploid structural chromosome rearrangements and mental subnormality in humans. | Q52116344 | ||
| Localization of the genes of 28S and 18S RNA in human somatic chromosomes by in situ hybridization | Q52852402 | ||
| An unbalanced 4q-21q translocation identified by the R but not by the G and Q chromosome banding techniques. | Q53787494 | ||
| T (14q-; 21q + ) translocation in the father. Partial trisomy 14 and monosomy 21 in the daughter | Q53796668 | ||
| Chromosomal aspects of human male sterility. | Q53894148 | ||
| Proceedings: Location of the genes for 5S RNA in the human chromosome complement. | Q54180889 | ||
| Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22) | Q66877977 | ||
| Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11) | Q66879734 | ||
| Trisomy 10q24--10qter | Q66882940 | ||
| Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case | Q66884587 | ||
| Partial trisomy of the long arm of the chromosme 11 by malsegregation of a maternal translocation t(11;22)(q23 1;q1 11) | Q66887377 | ||
| [Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)] | Q67257036 | ||
| Partial trisomy 11q and familial translocation 11--22 (author's transl) | Q67315112 | ||
| A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities | Q67323580 | ||
| Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1 | Q67432394 | ||
| Studies of the meiotic behavior of a translocation t(10;13)(q25;q11) in an oligospermic man | Q67713884 | ||
| [Bilateral anophthalmos. Facial anomalies and t(4;14) translocation] | Q68900196 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | chromosomal translocation | Q916504 |
| P304 | page(s) | 259-282 | |
| P577 | publication date | 1978-12-01 | |
| 1978-12-29 | |||
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Systematic analysis of 95 reciprocal translocations of autosomes | |
| P478 | volume | 45 |
| Q33671588 | A familial insertion involving an active nucleolar organiser within chromosome 12 |
| Q33673389 | A paracentric inversion of 7q illustrating a possible interchromosomal effect |
| Q71096226 | Abnormal phenotype in a child with the same balanced translocation (5;7)(p15;q22) as his father |
| Q40323919 | Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature |
| Q33676691 | Are double translocations double trouble? |
| Q40281369 | Arrangement of chromatin in the nucleus |
| Q43486626 | Breakpoint distribution in constitutional chromosome rearrangements with respect to fragile sites |
| Q83069838 | Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4) |
| Q48064539 | Cartographic study: breakpoints in 1574 families carrying human reciprocal translocations |
| Q34154155 | Chromosomal evolution in Primates: Tentative phylogeny from Microcebus murinus (Prosimian) to man |
| Q35202068 | Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases |
| Q40178026 | Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis |
| Q35197297 | Comparative mapping of the constitutional and tumor-associated 11;22 translocations |
| Q68624543 | Cytogenetic analysis of 400 sperm from three translocation heterozygotes |
| Q67980051 | Cytogenetic analysis of sperm from a male heterozygous for a 13;14 Robertsonian translocation |
| Q36711028 | Cytogenetic determinants of male fertility |
| Q71259733 | Cytogenetic survey in couples with recurrent fetal wastage |
| Q30445573 | De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints |
| Q70110354 | Deletion of band 13q21 is compatible with normal phenotype |
| Q52642412 | Different break-points in Philadelphia chromosome variant translocations and in constitutional and sporadic translocations. |
| Q35248011 | Direct segregation analysis of reciprocal translocations: a study of 283 sperm karyotypes from four carriers |
| Q35202630 | Distribution of break points in human structural rearrangements. |
| Q71142634 | Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling |
| Q52089146 | Excess of mental retardation and/or congenital malformation in reciprocal translocations in man. |
| Q41934361 | Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the down syndrome |
| Q71144116 | Fragile chromosome 16(q22) cause a balanced translocation at the same point |
| Q41546623 | Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase B |
| Q53652979 | Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes. |
| Q72032778 | Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)] |
| Q40814749 | Genome organization and species formation in vertebrates |
| Q71764578 | High-resolution chromosome analysis of phenotypically abnormal patients with apparently balanced structural rearrangements |
| Q40958521 | Impact of rearrangements on function and position of chromosomes in the interphase nucleus and on human genetic disorders |
| Q70795660 | Incomplete trisomy 22. III. Mosaic-trisomy 22 and the problem of full trisomy 22 |
| Q33703747 | Ionizing radiation and genetic risks. X. The potential "disease phenotypes" of radiation-induced genetic damage in humans: perspectives from human molecular biology and radiation genetics |
| Q41934601 | Is a gene for microcephaly located on chromosome 1? |
| Q71080041 | Malformation syndrome of duplication 12q24.1→qter |
| Q35249438 | Meiotic segregation, recombination, and gamete aneuploidy assessed in a t(1;10)(p22.1;q22.3) reciprocal translocation carrier by three- and four-probe multicolor FISH in sperm |
| Q52091708 | Mentally retarded siblings with congenital heart defect, peculiar facies and cryptorchidism in the male: possible McDonough syndrome with coincidental (X; 20) translocation |
| Q81631790 | Negligible interchromosomal effect in embryos of Robertsonian translocation carriers |
| Q35195124 | No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangements |
| Q90419741 | Non-Random Distribution of Reciprocal Translocation Breakpoints in the Pig Genome |
| Q70683932 | Nonrandom distribution of exchange points in patients with reciprocal translocations |
| Q33671846 | Partial trisomy 12q24.31----qter |
| Q33670243 | Partial trisomy 12q: a clinically recognisable syndrome. Genetic risks associated with translocations of chromosome 12q. |
| Q40218333 | Pericentric inversions of chromosome 12 in two families |
| Q41587054 | Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases |
| Q33858951 | Prader-Willi syndrome: current understanding of cause and diagnosis |
| Q37845069 | Predisposition to aneuploidy in the oocyte |
| Q81318818 | Preferential alternate segregation in the common t(11;22)(q23;q11) reciprocal translocation: sperm FISH analysis in two brothers |
| Q68007669 | Segregation analysis and genetic counseling when both parents carry balanced chromosomal translocations |
| Q35247998 | Segregation analysis of translocations by the study of human sperm chromosome complements |
| Q71397691 | Semen analysis in subfertile balanced-translocation carriers |
| Q33673734 | Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2) |
| Q26773011 | Somatic/gonadal mosaicism for structural autosomal rearrangements: female predominance among carriers of gonadal mosaicism for unbalanced rearrangements |
| Q50794510 | Sperm chromosome complements from two human reciprocal translocation heterozygotes |
| Q70789175 | Sperm nuclei analysis of a Robertsonian t(14q21q) carrier, by FISH, using three plasmids and two YAC probes |
| Q33674886 | Structural rearrangements in the parents of children with primary trisomy 21. |
| Q70884050 | Tentative estimate of the risk of chromosomal disease due to radiation-induced translocations in man |
| Q68433216 | The association of t (13q, 14q) with Down's syndrome and its inheritance |
| Q44051136 | The pattern of radiation-induced transmissible aberrations in a human cell culture |
| Q71429068 | The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation |
| Q33671782 | The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect? |
| Q70943649 | Translocations involving chromosome 12. I. A report of a 12,21 translocation in a woman with recurrent abortions, and a study of the breakpoints and modes of ascertainment of translocations involving chromosome 12 |
| Q71065652 | Translocations of chromosome 12. II. A comparison of the distribution of sites of spontaneous and induced breakages |
| Q78010936 | Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up |
| Q44596981 | Two familial 9;17 translocations with variable effect on male carriers fertility |
| Q71240314 | Two reciprocal translocations t(9p+;13q-) and t(13q-;21q+): a study of the families |
| Q60035790 | Unicolor and bicolor in situ hybridization in the diagnosis of peripheral neuroepithelioma and related tumors |
| Q70542186 | X-autosome translocations: cytogenetic characteristics and their consequences |
| Q37514731 | Z-DNA immunoreactivity in fixed metaphase chromosomes of primates |
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