Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype-Reference-Cited by-同舟云学术

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Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype

Published:2005-06-03 Issue:S7 Volume:37 Page:110-114
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Williams Charles A.,Frias Jaime L.,McCormick Mary Kay,Antonarakis Stylianos E.,Cantu Eduardo S.

Publisher

Wiley

Subject

Genetics (clinical)

Reference21 articles.

1. An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes;Bloom;Hum Genet,1976

2. Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21);Couturier;Hum Genet,1979

3. Submicroscopic duplication of chromosome 21 and trisomy 21 phenotype (Down syndrome);Delabar;Hum Genet,1987

4. Moderate Down's syndrome in three siblings having partial trisomy 21q22. 2qter and therefore no SOD-1 excess;Habedank;Hum Genet,1982

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mental Retardation: Genetic Findings, Clinical Implications and Research Agenda;Journal of Child Psychology and Psychiatry;1996-03

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