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2D and 3D Ultrasonographic Evaluation of Fetal Midface Hypoplasia in Two Cases with 3-M Syndrome.A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene.3-M syndrome: a novel CUL7 mutation associated with respiratory distress and a good response to GH therapy.An adult with 3-M syndrome.
P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
name
3M syndrome: a report of four cases in two families
@ast
3M syndrome: a report of four cases in two families
@en
type
label
3M syndrome: a report of four cases in two families
@ast
3M syndrome: a report of four cases in two families
@en
prefLabel
3M syndrome: a report of four cases in two families
@ast
3M syndrome: a report of four cases in two families
@en
P2860
P356
P1476
3M syndrome: a report of four cases in two families
@en
P2093
Ayla Güven
Ayşe Nurcan Cebeci
P2860
P304
P356
10.4274/JCRPE.V3I3.30
P577
2011-01-01T00:00:00Z