Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients

American Journal of Human Genetics

Volumn 59, Issue 2, 1996, Pages 417-422

  Shimkets, Richard ^a   Gailani, Mae R ^a   Siu, Victoria M ^b   Yang Feng, Theresa ^a   Pressman, Carolyn L ^a   Levanat, Sonja ^a   Goldstein, Alisa ^c   Dean, Michael ^d   Bale, Allen E ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF WESTERN ONTARIO   (Canada)

^c NATIONAL CANCER INSTITUTE   (United States)

^d NATIONAL CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADOLESCENT; ADULT; ARTICLE; BASAL CELL CARCINOMA; BASAL CELL NEVUS SYNDROME; CASE REPORT; CHROMOSOME 9Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME MAP; CONDUCTION DEAFNESS; DEVELOPMENTAL DISORDER; FAILURE TO THRIVE; FEMALE; FIBROMA; GENE REPRESSION; HUMAN; MEDULLOBLASTOMA; MENTAL DEFICIENCY; PHENOTYPE; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; TUMOR SUPPRESSOR GENE;

ADOLESCENT; ADULT; BASAL CELL NEVUS SYNDROME; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; HUMANS; KARYOTYPING; MALE; MEIOSIS; POLYMORPHISM, GENETIC; SEQUENCE DELETION;

EID: 0029790437     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. Albrecht S, von Deimling A, Pietsch T, Giangaspero F, Brandner S, Kleihues P, Wiestler OD (1994) Microsatellite analysis of loss of heterozygosity on chromosomes 9p, 11p and 17p in medulloblastoma. Neuropathol Appl Neurobiol 20:74-81
2. Anderson DE, Taylor WB, Falls HF, Davidson RT (1967) The nevoid basal cell carcinoma syndrome. Am J Hum Genet 19:12-22
3. Bale AE, Gailani MR, Leffell DJ (1994) The nevoid basal cell carcinoma syndrome. J Invest Dermatol Suppl 103:126S-130S
4. Bare JW, Xie J, Quinn AG, Epstein EH Jr (1995) Analysis of the FACC and XPAC genes as candidate genes for the basal cell nevus syndrome. Am J Hum Genet Suppl 57:A60
5. Bialer MG, Gailani MR, McLaughlin JA, Petrikovsky B, Bale AE (1994) Prenatal diagnosis of Gorlin syndrome. Lancet 344:477