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Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger-Huët anomalyClinical utility gene card for: 3-M syndrome - update 2013.Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome2D and 3D Ultrasonographic Evaluation of Fetal Midface Hypoplasia in Two Cases with 3-M Syndrome.Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in Asia.Clinical utility gene card for: 3M syndrome.
P2860
description
2000 nî lūn-bûn
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2000年の論文
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2000年学术文章
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2000年学术文章
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name
3-M syndrome: a prenatal ultrasonographic diagnosis.
@en
3-M syndrome: a prenatal ultrasonographic diagnosis.
@nl
type
label
3-M syndrome: a prenatal ultrasonographic diagnosis.
@en
3-M syndrome: a prenatal ultrasonographic diagnosis.
@nl
prefLabel
3-M syndrome: a prenatal ultrasonographic diagnosis.
@en
3-M syndrome: a prenatal ultrasonographic diagnosis.
@nl
P2093
P1433
P1476
3-M syndrome: a prenatal ultrasonographic diagnosis.
@en
P2093
P304
P356
10.1002/1097-0223(200011)20:11<921::AID-PD947>3.3.CO;2-2
P577
2000-11-01T00:00:00Z