A novel immunodeficiency syndrome associated with partial trisomy 19p13-Reference-Cited by-同舟云学术

A novel immunodeficiency syndrome associated with partial trisomy 19p13

Published:2014-01-15 Issue:4 Volume:51 Page:254-263
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Seidel Markus G,Duerr Celia,Woutsas Stavroula,Schwerin-Nagel Anette,Sadeghi Kambis,Neesen Jürgen,Uhrig Sabine,Santos-Valente Elisangela,Pickl Winfried F,Schwinger Wolfgang,Urban Christian,Boztug Kaan,Förster-Waldl Elisabeth

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference43 articles.

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4. Pure terminal duplication of the short arm of chromosome 19 in a boy with mild microcephaly;Andries;J Med Genet,2002

5. Array-CGH detection of a de novo 0.7-Mb deletion in 19p13.13 including CACNA1A associated with mental retardation and epilepsy with infantile spasms;Auvin;Epilepsia,2009

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