Literature DB >> 13935668

A chromosome abnormality with fragment in a paramongol child.

B R MIGEON, B N KAUFMANN, W J YOUNG.   

Abstract

Entities:  

Keywords:  CHROMOSOMES; MONGOLISM

Mesh：

Year:  1962        PMID： 13935668

Source DB:  PubMed          Journal:  Bull Johns Hopkins Hosp        ISSN： 0097-1383


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  4 in total

1.  Atypical acrocentric chromosomes in Negro and Caucasian Mongols.

Authors:  M N Starkman; M W Shaw
Journal:  Am J Hum Genet       Date:  1967-03       Impact factor: 11.025

2.  An extra chromosomal centric fragment in an infant with stigmata of Down's syndrome.

Authors:  I Subrt; H Prchlíková
Journal:  J Med Genet       Date:  1970-12       Impact factor: 6.318

3.  Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21.

Authors:  J D Williams; R L Summitt; P R Martens; R A Kimbrell
Journal:  Am J Hum Genet       Date:  1975-07       Impact factor: 11.025

4.  Systematic reanalysis of partial trisomy 21 cases with or without Down syndrome suggests a small region on 21q22.13 as critical to the phenotype.

Authors:  Maria Chiara Pelleri; Elena Cicchini; Chiara Locatelli; Lorenza Vitale; Maria Caracausi; Allison Piovesan; Alessandro Rocca; Giulia Poletti; Marco Seri; Pierluigi Strippoli; Guido Cocchi
Journal:  Hum Mol Genet       Date:  2016-04-22       Impact factor: 6.150
  4 in total

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