Literature DB >> 14063510

AUTOSOMAL DISORDERS.

J LEJEUNE.   

Abstract

Keywords:  CHROMOSOME ABNORMALITIES; REVIEW

Mesh：

Year:  1963        PMID： 14063510

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  41 in total

1.  Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families.

Authors:  J Boué; J L Taillemite; P Hazael-Massieux; C Léonard; A Boué
Journal:  Humangenetik       Date:  1975-09-20

2.  No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangements.

Authors:  A A Schinzel; P A Adelsberger; F Binkert; S Basaran; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

3.  Meiotic segregation and interchromosomal effects in a rare (1:2:10) complex chromosomal rearrangement.

Authors:  Gordon Kirkpatrick; Sai Ma
Journal:  J Assist Reprod Genet       Date:  2011-11-22       Impact factor: 3.412

4.  Triploidy arising from a first meiotic non-disjunction in a mother carrying a reciprocal translocation.

Authors:  L Rochon; M J Vekemans
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

5.  Human sperm chromosome studies in a reciprocal translocation t(2;5).

Authors:  C Templado; J Navarro; J Benet; A Genescà; M M Pérez; J Egozcue
Journal:  Hum Genet       Date:  1988-05       Impact factor: 4.132

6.  Unusual segregation products in sperm from a pericentric inversion 17 heterozygote.

Authors:  Monica M Mikhaail-Philips; Barbara C McGillivray; Sara J Hamilton; Evelyn Ko; Judy Chernos; Alfred Rademaker; Renée H Martin
Journal:  Hum Genet       Date:  2005-05-28       Impact factor: 4.132

7.  A satellited Yq chromosome associated with trisomy 21 and an inversion of chromosome 9.

Authors:  P N Howard-Peebles; G R Stoddard
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

8.  Down's syndrome with XYY additional aneuploidy.

Authors:  C Stoll; D Frey; D Willard; J Messer
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

9.  Sequential FISH allows the determination of the segregation outcome and the presence of numerical anomalies in spermatozoa from a t(1;8;2)(q42;p21;p15) carrier.

Authors:  Anna Godo; Joan Blanco; Francesca Vidal; Mònica Parriego; Montserrat Boada; Ester Anton
Journal:  J Assist Reprod Genet       Date:  2013-08-23       Impact factor: 3.412

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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