Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
about
Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication.Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas.Invited commentary: The need for human genetics and genomics in dental school curricula.Bone fracture healing in mechanobiological modeling: A review of principles and methods.Fgf3 and Fgf16 expression patterns define spatial and temporal domains in the developing chick inner ear.Identification of a second HOXA2 nonsense mutation in a family with autosomal dominant non-syndromic microtia and distinctive ear morphology.
P2860
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
@ast
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
@en
type
label
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
@ast
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
@en
prefLabel
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
@ast
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
@en
P2093
P2860
P356
P1433
P1476
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
@en
P2093
Andrew J Griffith
Byung Yoon Choi
Idrees Nasir
Rashmi S Hegde
Saima Riazuddin
Shaheen N Khan
Sheikh Riazuddin
Thomas B Friedman
Uzma Shaukat
Zubair M Ahmed
P2860
P2888
P356
10.1186/1471-2350-12-21
P577
2011-02-09T00:00:00Z