Prenatal diagnosis of Carpenter syndrome: Looking beyond craniosynostosis and polysyndactyly
Author:
Affiliation:
1. Department of Medical & Molecular Genetics; Indiana University School of Medicine; Indianapolis Indiana
2. Prenatal Diagnosis Clinic, Department of Obstetrics and Gynecology; Indiana University School of Medicine; Indianapolis IN
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36362/fullpdf
Reference14 articles.
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2. RAB23 mutation in a large family from Comoros islands with Carpenter syndrome;Alessandri;Am J Med Genet Part A,2010
3. The association of Carpenter syndrome and situs inversus totalis: First case report;Altunhan;Turkiye Klinikleri J Med Sci,2011
4. Prenatal sonographic diagnosis of Carpenter syndrome;Ashby;J Ultrasound Med,1994
5. A case of Carpenter syndrome diagnosed in a 20-week-old fetus with postmortem examination;Balci;Clin Genet,1997
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