Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours

Oncogene

Volumn 15, Issue 3, 1997, Pages 361-366

  Vorechovsky I ^a,b   Tingby, O ^c   Hartman, M ^d   Stromberg B ^e   Nister, M ^d   Collins, V P ^c   Toftgard R ^a  

^a KAROLINSKA INSTITUTE   (Sweden)

^b ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

^c KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^d UPPSALA UNIVERSITY HOSPITAL   (Sweden)

^e Department of Paediatrics ^*

Author keywords

Chromosome 9; Medulloblastoma; Mutation; Nevoid basal cell carcinoma syndrome; Patched; PTCH

Indexed keywords

DNA;

ARTICLE; BASAL CELL NEVUS SYNDROME; CANCER CELL CULTURE; CANCER GENETICS; CHROMOSOME 9Q; CLINICAL ARTICLE; CONTROLLED STUDY; DROSOPHILA; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; MEDULLOBLASTOMA; MISSENSE MUTATION; NEUROECTODERM TUMOR; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SINGLE STRAND CONFORMATION POLYMORPHISM; SOMATIC MUTATION; TUMOR SUPPRESSOR GENE;

ERINACEIDAE;

EID: 0030874617     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.onc.1201340     Document Type: Article

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