Literature DB >> 15151556

Finlay-Marks syndrome: another sporadic case and additional manifestations.

Hiroko Taniai1, Harold Chen, Susonne Ursin.   

Abstract

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Year:  2004        PMID: 15151556     DOI: 10.1111/j.1442-200x.2004.01905.x

Source DB:  PubMed          Journal:  Pediatr Int        ISSN: 1328-8067            Impact factor:   1.524


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  2 in total

1.  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

2.  Lactation and neonatal nutrition: defining and refining the critical questions.

Authors:  Margaret C Neville; Steven M Anderson; James L McManaman; Thomas M Badger; Maya Bunik; Nikhat Contractor; Tessa Crume; Dana Dabelea; Sharon M Donovan; Nicole Forman; Daniel N Frank; Jacob E Friedman; J Bruce German; Armond Goldman; Darryl Hadsell; Michael Hambidge; Katie Hinde; Nelson D Horseman; Russell C Hovey; Edward Janoff; Nancy F Krebs; Carlito B Lebrilla; Danielle G Lemay; Paul S MacLean; Paula Meier; Ardythe L Morrow; Josef Neu; Laurie A Nommsen-Rivers; Daniel J Raiten; Monique Rijnkels; Victoria Seewaldt; Barry D Shur; Joshua VanHouten; Peter Williamson
Journal:  J Mammary Gland Biol Neoplasia       Date:  2012-07-01       Impact factor: 2.673

  2 in total

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