DLL3 as a candidate gene for vertebral malformations-Reference-Cited by-同舟云学术

DLL3 as a candidate gene for vertebral malformations

Published:2006 Issue:22 Volume:140A Page:2447-2453
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Giampietro Philip F.,Raggio Cathleen L.,Reynolds Cory,Ghebranious Nader,Burmester James K.,Glurich Ingrid,Rasmussen Kristen,McPherson Elizabeth,Pauli Richard M.,Shukla Sanjay K.,Merchant Sajid,Jacobsen F. Stig,Faciszewski Thomas,Blank Robert D.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference30 articles.

1. Wnt3a Plays a Major Role in the Segmentation Clock Controlling Somitogenesis

2. Valproic Acid and Congenital Malformations

3. Mutations in the human Delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis

4. VACTERL with the mitochondrial NP 3243 point mutation

5. Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene

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