Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay-Reference-Cited by-同舟云学术

Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay

Published:2011-12-21 Issue:2 Volume:158A Page:391-399
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Muller Eric A.,Aradhya Swaroop,Atkin Joan F.,Carmany Erin P.,Elliott Alison M.,Chudley Albert E.,Clark Robin D.,Everman David B.,Garner Shannon,Hall Bryan D.,Herman Gail E.,Kivuva Emma,Ramanathan Subhadra,Stevenson David A.,Stockton David W.,Hudgins Louanne

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference31 articles.

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3. Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3->q31.3) associated with Gorlin syndrome;Chen;Prenat Diagn,2006

4. Early detection of chromosome 9q22.32q31.1 microdeletion and the nevoid basal cell carcinoma syndrome;de Ravel;Eur J Med Genet,2009

5. PTCH1 duplication in a family with microcephaly and mild developmental delay;Derwinska;Eur J Hum Genet,2009

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