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split-hand/foot malformation
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DLX5
Association by guilt: identification of DLX5 as a target for MeCP2 provides a molecular link between genomic imprinting and Rett syndrome
Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly
TP63
P63 alpha mutations lead to aberrant splicing of keratinocyte growth factor receptor in the Hay-Wells syndrome
A skin microRNA promotes differentiation by repressing 'stemness'
miRNAs, 'stemness' and skin
WNT10B
Isolation, characterization and chromosomal localization of human WNT10B
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Pathways in cancer
Homo sapiens (human)
one gene
Cancer Gene Census
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TP63
Somatic tumors
HNSCC, DLBCL
Tumor types germline
NSCLC
Cancer Syndrom
Translocation partner
TBL1XR1
Name
tumor protein p63
Chromosome banding
3q28
Cancer molecular gen.
Mutation type
Mis, N, T
Other syndrome disease
associated with Hay-Wells syndrome, ADULT syndrome, ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome (EEC), acro-dermato-ungual-lacrimal-tooth syndrome, limb mammary syndrome, Rapp-Hodgkin syndrome, split hand-split foot malformation
Clinical Trials
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