Gorlin-chaudhry-moss syndrome revisited: Expanding the phenotype-Reference-Cited by-同舟云学术

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Gorlin-chaudhry-moss syndrome revisited: Expanding the phenotype

Published:2013-05-17 Issue:7 Volume:161 Page:1737-1742
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Rosti Rasim O.¹,Karaer Kadri¹,Karaman Birsen²,Torun Deniz¹,Guran Sefik³,Bahce Muhterem¹

Affiliation:

1. Department of Medical Genetics; Gulhane Military Medical Academy; Ankara; Turkey

2. Department of Medical Genetics; Istanbul Medical Faculty Istanbul University; Istanbul; Turkey

3. Department of Medical Biology; Gulhane Military Medical Academy; Ankara; Turkey

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35954/fullpdf

Reference5 articles.

1. Two sisters resembling Gorlin-Chaudhry-Moss syndrome;Aravena;Am J Med Genet Part A,2011

2. Craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies-A new syndrome;Gorlin;J Pediatr,1960

3. Craniofacial dysostosis, hypertrichosis, genital hypoplasia, ocular, dental, and digital defects: Confirmation of the Gorlin-Chaudhry-Moss syndrome;Ippel;Am J Med Genet,1992

4. Previously unrecognized congenital progeroid disorder;Petty;Am J Med Genet,1990

5. Gorlin-Chaudhry-Moss or Saethre-Chotzen syndrome;Preis;Clin Genet,1995

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5. Hypertrichosis in Childhood;Turkish Journal of Dermatology / Türk Dermatoloji Dergisi;2018-04-02

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