NBCCS secondary to an interstitial chromosome 9q deletion

Clinical and Experimental Dermatology

Volumn 29, Issue 5, 2004, Pages 542-544

  Haniffa, M A ^a   Leech, S N ^a   Lynch, S A ^b   Simpson, N B ^a  

^a ROYAL VICTORIA INFIRMARY   (United Kingdom)

^b NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BASAL CELL NEVUS SYNDROME; CASE REPORT; CHROMOSOME 9Q; DEVELOPMENTAL DISORDER; FEMALE; GENE; GENE MUTATION; HUMAN; HYPOTELORISM; INTERSTITIAL CHROMOSOME DELETION; PHENOTYPE; PRIORITY JOURNAL; PTCH1 GENE; RARE DISEASE; SHORT STATURE;

ADULT; BASAL CELL NEVUS SYNDROME; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; GERM-LINE MUTATION; HUMANS; KARYOTYPING; PHENOTYPE;

EID: 4644312365     PISSN: 03076938     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-2230.2004.01590.x     Document Type: Article

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