A novel mutation of HOXA13 in a family with hand-foot-genital syndrome and the role of polyalanine expansions in the spectrum of Müllerian fusion anomalies
about
Structural basis for sequence specific DNA binding and protein dimerization of HOXA13Tandem amino acid repeats in the green anole (Anolis carolinensis) and other squamates may have a role in increasing genetic variabilityBackbone chemical shift assignments of mouse HOXA13 DNA binding domain bound to duplex DNA.Chemical shift assignments of mouse HOXD13 DNA binding domain bound to duplex DNA.7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype.Etiologies of uterine malformations.
P2860
A novel mutation of HOXA13 in a family with hand-foot-genital syndrome and the role of polyalanine expansions in the spectrum of Müllerian fusion anomalies
description
2009 nî lūn-bûn
@nan
2009 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2009年の論文
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2009年学术文章
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2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
name
A novel mutation of HOXA13 in ...... of Müllerian fusion anomalies
@ast
A novel mutation of HOXA13 in ...... of Müllerian fusion anomalies
@en
type
label
A novel mutation of HOXA13 in ...... of Müllerian fusion anomalies
@ast
A novel mutation of HOXA13 in ...... of Müllerian fusion anomalies
@en
prefLabel
A novel mutation of HOXA13 in ...... of Müllerian fusion anomalies
@ast
A novel mutation of HOXA13 in ...... of Müllerian fusion anomalies
@en
P2093
P2860
P1476
A novel mutation of HOXA13 in ...... of Müllerian fusion anomalies
@en
P2093
Elisa M Jorgensen
Hugh S Taylor
Jane I Ruman
Leo Doherty
P2860
P304
P356
10.1016/J.FERTNSTERT.2009.05.057
P407
P577
2009-07-09T00:00:00Z