A progeroid syndrome with neonatal presentation and long survival maps to 19p13.3p13.2-Reference-Cited by-同舟云学术

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A progeroid syndrome with neonatal presentation and long survival maps to 19p13.3p13.2

Published:2013-05-20 Issue:7 Volume:97 Page:456-462
ISSN:1542-0752
Container-title:Birth Defects Research Part A: Clinical and Molecular Teratology
language:en
Short-container-title:Birth Defects Research Part A: Clinical and Molecular Teratology

Author:

Akawi Nadia¹,Ali Bassam¹,Al Gazali Lihadh²

Affiliation:

1. Department of Pathology; College of Medicine and Health Sciences, United Arab Emirates University; Al-Ain United Arab Emirates

2. Department of Paediatrics; College of Medicine and Health Sciences, United Arab Emirates University; Al-Ain United Arab Emirates

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Reference36 articles.

1. Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia;Agarwal;Hum Mol Genet,2003

2. Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE);Al-Gazali;Hum Mutat,2010

3. Follow-up study of Wiedemann-Rautenstrauch syndrome: long-term survival and comparison with Rautenstrauch's patient “G”;Arboleda;Birth Defects Res A Clin Mol Teratol,2005

4. Wiedemann-Rautenstrauch neonatal progeroid syndrome: report of three new patients;Arboleda;J Med Genet,1997

5. Neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome): report of three affected sibs;Arboleda;Am J Med Genet A,2011

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