Intra-familial variability of ectodermal defects associated with WNT10A mutations

Acta Dermato-Venereologica

Volumn 91, Issue 3, 2011, Pages 346-347

  Wedgeworth, Emma K ^a   Nagy, Nikoletta ^b   White, Jonathan M L ^a   Pembroke, Andrew C ^c   McGrath, John A ^a,b,d  

^a GUY'S AND ST THOMAS' NHS FOUNDATION TRUST   (United Kingdom)

^b KING'S COLLEGE LONDON   (United Kingdom)

^c KENT COMMUNITY HEALTH NHS FOUNDATION TRUST   (United Kingdom)

^d GUY S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; WNT10A PROTEIN;

CASE REPORT; DNA SCREENING; ECTODERMAL DYSPLASIA; GENE AMPLIFICATION; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HIDRADENOMA; HUMAN; LETTER; ODONTO ONYCHO DERMAL DYSPLASIA; PRIORITY JOURNAL; SCHOPF SCHULZ PASSARGE SYNDROME;

DNA MUTATIONAL ANALYSIS; ECTODERMAL DYSPLASIA; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HAIR; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MALE; MUTATION; NAILS; PEDIGREE; PHENOTYPE; SKIN; TOOTH DISEASES; WNT PROTEINS;

EID: 79955719427     PISSN: 00015555     EISSN: None     Source Type: Journal    
DOI: 10.2340/00015555-1028     Document Type: Letter

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