Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: Prenatal diagnosis and aCGH characterization using uncultured amniocytes-Reference-Cited by-同舟云学术

Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: Prenatal diagnosis and aCGH characterization using uncultured amniocytes

Published:2013-09 Issue:2 Volume:527 Page:636-641
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Chen Chih-Ping,Huang Jian-Pei,Chen Yi-Yung,Chern Schu-Rern,Wu Peih-Shan,Su Jun-Wei,Pan Chen-Wen,Wang Wayseen

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference58 articles.

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4. Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation;Brenk;Eur. J. Hum. Genet.,2007

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