Literature DB >> 5310102

[Study of progeny of individuals bearing a t(DqDq) translocation].

B Dutrillaux, J Lejeune.   

Abstract

Mesh:

Year:  1970        PMID: 5310102

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


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  17 in total

1.  Analysis of meiotic segregation in a man heterozygous for a 13;15 Robertsonian translocation and a review of the literature.

Authors:  F Pellestor
Journal:  Hum Genet       Date:  1990-06       Impact factor: 4.132

2.  Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 Robertsonian translocation.

Authors:  F Pellestor; B Sele; H Jalbert
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

3.  A pericentric inversion of a chromosome 4 with a t(4q+10p-) and a familial t(DqDq) in a mentally retarded girl.

Authors:  S W Soukup; W Yarema; M Robinow
Journal:  Humangenetik       Date:  1974

4.  [Comparison of the structure of chromatids of Homo sapiens and Pan troglodytes (author's transl)].

Authors:  J Lejeune; B Dutrillaux; M O Rethoré; M Prieur
Journal:  Chromosoma       Date:  1973       Impact factor: 4.316

5.  D-D translocations in males examined for military service.

Authors:  E Zeuthen; J Nielsen
Journal:  J Med Genet       Date:  1973-12       Impact factor: 6.318

Review 6.  Down's syndrome. Current stage of cytogenetic research.

Authors:  M Mikkelsen
Journal:  Humangenetik       Date:  1971

7.  Identification of a familial Robertsonian translocation t(13q14q) by means of thermic moderated denaturation.

Authors:  C Stoll; J M Levy
Journal:  Humangenetik       Date:  1973-07-20

8.  Three generations and six family members with a t(13q15q) chromosome.

Authors:  R L Neu; L I Gardner; M L Williams; M J Barlow
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

9.  [Chromosome studies in couples with repeated abortions].

Authors:  H D Rott; E Richter; W D Rummel; G Schwanitz
Journal:  Arch Gynakol       Date:  1972

10.  Two cases of familial paracentric inversion in man associated with sex chromosome anomaly. 47,XXY,inv(5)(q21q32) and 45,X,inv(7)(q11.3q22.3).

Authors:  N Canki; B Dutrillaux
Journal:  Hum Genet       Date:  1979-04-05       Impact factor: 4.132

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