Severe Developmental Delay in a Patient with 7p21.1-p14.3 Microdeletion Spanning the TWIST Gene and the HOXA Gene Cluster.
about
HOXA genes cluster: clinical implications of the smallest deletion.Epigenetic inactivation of HOXA11, a novel functional tumor suppressor for renal cell carcinoma, is associated with RCC TNM classification.Severe persistent pulmonary hypertension of the newborn and dysmorphic features in neonate with a deletion involving TWIST1 and PHF14: a case report.7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype.Genetic advances in craniosynostosis.
P2860
Severe Developmental Delay in a Patient with 7p21.1-p14.3 Microdeletion Spanning the TWIST Gene and the HOXA Gene Cluster.
description
2011 nî lūn-bûn
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2011年の論文
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2011年論文
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2011年論文
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2011年論文
@zh-hk
2011年論文
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2011年論文
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2011年论文
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name
Severe Developmental Delay in ...... ene and the HOXA Gene Cluster.
@en
Severe Developmental Delay in ...... ene and the HOXA Gene Cluster.
@nl
type
label
Severe Developmental Delay in ...... ene and the HOXA Gene Cluster.
@en
Severe Developmental Delay in ...... ene and the HOXA Gene Cluster.
@nl
prefLabel
Severe Developmental Delay in ...... ene and the HOXA Gene Cluster.
@en
Severe Developmental Delay in ...... ene and the HOXA Gene Cluster.
@nl
P2093
P2860
P356
P1476
Severe Developmental Delay in ...... Gene and the HOXA Gene Cluster
@en
P2093
A Kattamis
E Kanavakis
H Fryssira
K Stokidis
P2860
P356
10.1159/000334313
P577
2011-11-12T00:00:00Z