Sensorineural deafness, distinctive facial features, and abnormal cranial bones: a new variant of Waardenburg syndrome?
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PAX3 gene deletion detected by microarray analysis in a girl with hearing lossA novel missense mutation of the paired box 3 gene in a Turkish family with Waardenburg syndrome type 1.Heritabilities of facial measurements and their latent factors in korean families.Pigmentation PAX-ways: the role of Pax3 in melanogenesis, melanocyte stem cell maintenance, and diseaseAnterior ethmoidal artery emerging anterior to bulla ethmoidalis: An abnormal anatomical variation in Waardenburg's syndrome.A novel mutation in PAX3 associated with Waardenburg syndrome type I in a Chinese family
P2860
Sensorineural deafness, distinctive facial features, and abnormal cranial bones: a new variant of Waardenburg syndrome?
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Sensorineural deafness, distin ...... riant of Waardenburg syndrome?
@en
Sensorineural deafness, distin ...... riant of Waardenburg syndrome?
@nl
type
label
Sensorineural deafness, distin ...... riant of Waardenburg syndrome?
@en
Sensorineural deafness, distin ...... riant of Waardenburg syndrome?
@nl
prefLabel
Sensorineural deafness, distin ...... riant of Waardenburg syndrome?
@en
Sensorineural deafness, distin ...... riant of Waardenburg syndrome?
@nl
P2093
P2860
P356
P1476
Sensorineural deafness, distin ...... riant of Waardenburg syndrome?
@en
P2093
Kenneth R Maravilla
Mark Matsushita
Mercy Laurino
Wendy H Raskind
P2860
P304
P356
10.1002/AJMG.A.32402
P407
P577
2008-07-01T00:00:00Z