Publicações

The Origin of Efnb1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males

AuthID
P-004-K8V

Author(s)

Twigg, SRF

Matsumoto, K

Kidd, AMJ

Goriely, A

Taylor, IB

Fisher, RB

Hoogeboom, AJM

Mathijssen, IMJ

Lourenco, MT

Morton, JEV

Sweeney, E

Wilson, LC

Brunner, HG

Mulliken, JB

Wall, SA

Wilkie, AOM

Tipo de Documento

Article

Year published

2006

Publicado

in AMERICAN JOURNAL OF HUMAN GENETICS, ISSN: 0002-9297

Volume: 78, Número: 6, Páginas: 999-1010 (12)

Indexing

Wos^®

Scopus^®

Crossref^®

Pubmed^®

Google Scholar^®

Metadata
Fontes

Publication Identifiers

DOI: 10.1086/504440

Pubmed: 16685650

SCOPUS: 2-s2.0-33646879391

Wos: WOS:000237553800009

Source Identifiers

ISSN: 0002-9297

Export Publication Metadata

Lista Marked

Adicionar à lista Marked

Info

At this moment we don't have any links to full text documens.

The Origin of Efnb1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males

Links Úteis

Ajuda

Autenticação Federada (Clique na imagem)

The Origin of Efnb1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males

Links Úteis

Ajuda