Stüve-Wiedemann syndrome: update and historical footnote.
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Stüve-Wiedemann Syndrome: Update on Clinical and Genetic AspectsDifferential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disordersCase report of prenatal diagnosis of Stüve-Wiedemann Syndrome in a woman with another child affected too.Stüve-Wiedemann syndrome: LIFR and associated cytokines in clinical course and etiology.In vitro readthrough of termination codons by gentamycin in the Stüve-Wiedemann Syndrome.Congenital contractures and distinctive phenotypic features consistent with Stuve-Wiedmann syndrome in a male infant.
P2860
Stüve-Wiedemann syndrome: update and historical footnote.
description
1996 nî lūn-bûn
@nan
1996 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Stüve-Wiedemann syndrome: update and historical footnote.
@ast
Stüve-Wiedemann syndrome: update and historical footnote.
@en
Stüve-Wiedemann syndrome: update and historical footnote.
@nl
type
label
Stüve-Wiedemann syndrome: update and historical footnote.
@ast
Stüve-Wiedemann syndrome: update and historical footnote.
@en
Stüve-Wiedemann syndrome: update and historical footnote.
@nl
prefLabel
Stüve-Wiedemann syndrome: update and historical footnote.
@ast
Stüve-Wiedemann syndrome: update and historical footnote.
@en
Stüve-Wiedemann syndrome: update and historical footnote.
@nl
P1476
Stüve-Wiedemann syndrome: update and historical footnote.
@en
P2093
P356
10.1002/(SICI)1096-8628(19960503)63:1<12::AID-AJMG5>3.3.CO;2-R
P577
1996-05-01T00:00:00Z