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American Journal of Medical Genetics

Volumn 112, Issue 1, 2002, Pages 61-64

Complex karyotypic abnormality in ovarian fibroma associated with Gorlin syndrome

(4) Smith, Lynn M a Hu, Ping b Meyer, Larry J c Coffin, Cheryl M a,d

a UNIVERSITY OF UTAH HEALTH SCIENCES CENTER (United States)

b GERIATRIC RESEARCH EDUCATION AND CLINICAL CENTER (United States)

c UNIVERSITY OF UTAH SCHOOL OF MEDICINE (United States)

d PRIMARY CHILDREN'S MEDICAL CENTER (United States)

Author keywords

Gorlin syndrome; Nevoid basal cell carcinoma syndrome; Ovarian fibroma

Indexed keywords

ARTICLE; BASAL CELL NEVUS SYNDROME; CASE REPORT; CHILD; COMPUTER ASSISTED TOMOGRAPHY; CYTOGENETICS; DISEASE ASSOCIATION; FEMALE; GENE; GENE MUTATION; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; KARYOTYPE; OVARIECTOMY; OVARY TUMOR; PRIORITY JOURNAL; TUMOR BIOPSY; FIBROMA; GENETICS; KARYOTYPING; PATHOLOGY;

BASAL CELL NEVUS SYNDROME; CASE REPORT; CHILD; FEMALE; FIBROMA; HUMAN; KARYOTYPING; OVARIAN NEOPLASMS; HUMANS;

EID: 0037105016 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.10607 Document Type: Article

Times cited : (11)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.