Reconstructing the history of human limb development: lessons from birth defects.
about
The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome.Congenital thrombocytopenia and radio-ulnar synostosis: a new familial syndrome.Terminal osseous dysplasia with pigmentary defects maps to human chromosome Xq27.3-xqter.Characterization of limb differences in children with Cornelia de Lange Syndrome.
P2860
Reconstructing the history of human limb development: lessons from birth defects.
description
1999 nî lūn-bûn
@nan
1999 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի մարտին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Reconstructing the history of human limb development: lessons from birth defects.
@ast
Reconstructing the history of human limb development: lessons from birth defects.
@en
Reconstructing the history of human limb development: lessons from birth defects.
@nl
type
label
Reconstructing the history of human limb development: lessons from birth defects.
@ast
Reconstructing the history of human limb development: lessons from birth defects.
@en
Reconstructing the history of human limb development: lessons from birth defects.
@nl
prefLabel
Reconstructing the history of human limb development: lessons from birth defects.
@ast
Reconstructing the history of human limb development: lessons from birth defects.
@en
Reconstructing the history of human limb development: lessons from birth defects.
@nl
P2093
P2860
P1433
P1476
Reconstructing the history of human limb development: lessons from birth defects.
@en
P2093
Watkins WS
P2860
P304
P356
10.1203/00006450-199903000-00001
P407
P577
1999-03-01T00:00:00Z
P6179
1064214119