A new frontonasal dysplasia syndrome associated with deletion of theSIX2gene-Reference-Cited by-同舟云学术

A new frontonasal dysplasia syndrome associated with deletion of theSIX2gene

Published:2015-11-18 Issue:2 Volume:170 Page:487-491
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Hufnagel Robert B.¹,Zimmerman Sarah L.¹,Krueger Laura A.¹,Bender Patricia L.¹,Ahmed Zubair M.²,Saal Howard M.¹

Affiliation:

1. Division of Human Genetics; Cincinnati Children's Hospital Medical Center and Department of Pediatrics. University of Cincinnati College of Medicine; Cincinnati Ohio

2. Department of Otorhinolaryngology; University of Maryland; Baltimore Maryland

Funder

National Institute on Deafness and Other Communication Disorders (NIDCD/NIH)

Internal Departmental Funds

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference31 articles.

1. Severe nasal clefting and abnormal embryonic apoptosis in Alx3/Alx4 double mutant mice;Beverdam;Development,2001

2. Structure, mapping and expression of the human gene encoding the homeodomain protein, SIX2;Boucher;Gene,2000

3. Negative effect of Hox gene expression on the development of the neural crest-derived facial skeleton;Creuzet;Development,2002

4. Alx1, a member of the Cart1/Alx3/Alx4 subfamily of Paired-class homeodomain proteins, is an essential component of the gene network controlling skeletogenic fate specification in the sea urchin embryo;Ettensohn;Development,2003

5. Misexpression of Six2 is associated with heritable frontonasal dysplasia and renal hypoplasia in 3H1 Br mice;Fogelgren;Dev Dyn,2008

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