Mutations in KCTD1 Cause Scalp-Ear-Nipple Syndrome-Reference-Cited by-同舟云学术

Mutations in KCTD1 Cause Scalp-Ear-Nipple Syndrome

Published:2013-04 Issue:4 Volume:92 Page:621-626
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Marneros Alexander G.,Beck Anita E.,Turner Emily H.,McMillin Margaret J.,Edwards Matthew J.,Field Michael,de Macena Sobreira Nara Lygia,Perez Ana Beatriz A.,Fortes Jose A.R.,Lampe Anne K.,Giovannucci Uzielli Maria Luisa,Gordon Christopher T.,Plessis Ghislaine,Le Merrer Martine,Amiel Jeanne,Reichenberger Ernst,Shively Kathryn M.,Cerrato Felecia,Labow Brian I.,Tabor Holly K.,Smith Joshua D.,Shendure Jay,Nickerson Deborah A.,Bamshad Michael J.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference19 articles.

1. An hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples;Finlay;Br. J. Dermatol.,1978

2. Hypotonia, developmental delay and features of scalp-ear-nipple syndrome in an inbred Arab family;Al-Gazali;Clin. Dysmorphol.,2007

3. Hypothelia, syndactyly, and ear malformation—a variant of the scalp-ear-nipple syndrome?: Case report and review of the literature;Baris;Am. J. Med. Genet. A.,2005

4. Scalp-ear-nipple syndrome: additional manifestations;Edwards;Am. J. Med. Genet.,1994

5. Finlay-Marks syndrome: report of two siblings and review of literature;Naik;Am. J. Med. Genet. A.,2012

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