Literature DB >> 16411189

Finlay-Marks (SEN) syndrome: a sporadic case and the delineation of the syndrome.

Nara Lygia de Macena Sobreira, Décio Brunoni, Mirlene Cecília Soares Pinho Cernach, Ana Beatriz Alvarez Perez.   

Abstract

Entities:  

Mesh：

Year:  2006        PMID： 16411189     DOI： 10.1002/ajmg.a.31063

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


× No keyword cloud information.
  3 in total

Review 1.  Genetics of syndromic ocular coloboma: CHARGE and COACH syndromes.

Authors:  Aman George; Tiziana Cogliati; Brian P Brooks
Journal:  Exp Eye Res       Date:  2020-02-04       Impact factor: 3.467

2.  Mutations in KCTD1 cause scalp-ear-nipple syndrome.

Authors:  Alexander G Marneros; Anita E Beck; Emily H Turner; Margaret J McMillin; Matthew J Edwards; Michael Field; Nara Lygia de Macena Sobreira; Ana Beatriz A Perez; Jose A R Fortes; Anne K Lampe; Maria Luisa Giovannucci Uzielli; Christopher T Gordon; Ghislaine Plessis; Martine Le Merrer; Jeanne Amiel; Ernst Reichenberger; Kathryn M Shively; Felecia Cerrato; Brian I Labow; Holly K Tabor; Joshua D Smith; Jay Shendure; Deborah A Nickerson; Michael J Bamshad
Journal:  Am J Hum Genet       Date:  2013-03-28       Impact factor: 11.025

3.  Scalp-ear-nipple syndrome: a case report.

Authors:  Estela Morales-Peralta; Vivian Andrés; Dainé Campillo Betancourt
Journal:  Case Rep Med       Date:  2014-02-09
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.