P63 mutations are not a major cause of non-syndromic split hand/foot malformation [4]

Journal of Medical Genetics

Volumn 40, Issue 1, 2003, Pages 55-61

  De Mollerat, X J ^a   Everman, D B ^a   Morgan, C T ^a   Clarkson, K B ^a   Rogers, R C ^a   Colby, R S ^a   Aylsworth, A S ^b   Graham Jr , J M ^c   Stevenson, R E ^a   Schwartz, C E ^a  

^a GREENWOOD GENETIC CENTER   (United States)

^b UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BONE DEFECT; CANCER INHIBITION; CENTRAL NERVOUS SYSTEM; COLOBOMA; DISEASE ASSOCIATION; DNA BINDING; FOOT MALFORMATION; GENE EXPRESSION; GENE MUTATION; GENETIC CODE; HUMAN; HYDROCEPHALUS; LETTER; MICROCEPHALY; MICROPHTHALMIA; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NONHUMAN; PRIORITY JOURNAL;

DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; FEMALE; FOOT DEFORMITIES, CONGENITAL; GENES, TUMOR SUPPRESSOR; HAND DEFORMITIES, CONGENITAL; HUMANS; INFANT; MALE; MEMBRANE PROTEINS; MUTATION; PEDIGREE; PHOSPHOPROTEINS; SYNDROME; TRANS-ACTIVATORS; TUMOR SUPPRESSOR PROTEINS;

EID: 0037244668     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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