Literature DB >> 5454712

The G deletion syndromes.

R J Warren, D L Rimoin.   

Abstract

Mesh：

Year:  1970        PMID： 5454712     DOI： 10.1016/s0022-3476(70)80209-8

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  33 in total

1.  A male infant with monosomy 21.

Authors:  Y Kaneko; T Ikeuchi; M Sasaki; Y Stakae; S Kuwajima
Journal:  Humangenetik       Date:  1975-08-29

2.  Familial Ebstein's anomaly.

Authors:  A Rosenmann; I Arad; A Simcha; T Schaap
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

3.  A case of ring chromosome.

Authors:  D S Brookfield; S Walker
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

4.  Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion.

Authors:  J R Korenberg; D K Kalousek; G Anneren; S M Pulst; J G Hall; C J Epstein; D R Cox
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

5.  Molecular mechanism in the formation of a human ring chromosome 21.

Authors:  C Wong; H H Kazazian; G Stetten; W C Earnshaw; M L Van Keuren; S E Antonarakis
Journal:  Proc Natl Acad Sci U S A       Date:  1989-03       Impact factor: 11.205

6.  Chromosome survey of total population of mentally subnormal in North-East of Scotland.

Authors:  R M Speed; A W Johnston; H J Evans
Journal:  J Med Genet       Date:  1976-08       Impact factor: 6.318

7.  21 ring chromosome in a girl with stigmata of Down's and G deletion I syndromes.

Authors:  A Serra; D P Singh-Kahlon
Journal:  Hum Genet       Date:  1976-07-07       Impact factor: 4.132

8.  A female infant with monosomy 21.

Authors:  P Dziuba; D Dziekanowska; H Hübner
Journal:  Hum Genet       Date:  1976-03-12       Impact factor: 4.132

9.  Full monosomy 21: a clinically recognizable syndrome?

Authors:  J P Fryns; F D'Hondt; P Goddeeris; H van den Berghe
Journal:  Hum Genet       Date:  1977-06-30       Impact factor: 4.132

10.  Unbalanced 13q/21q translocation: a revised study of the case previously reported as 21-monosomy.

Authors:  T Ikeuchi; I Kondo; M Sasaki; Y Kaneko; S Kodama
Journal:  Hum Genet       Date:  1976-08-30       Impact factor: 4.132
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