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TUMORS IN RUBINSTEIN-TAYBI SYNDROME
Author(s): MILLER RW, RUBINSTEIN JH
Source: AMERICAN JOURNAL OF MEDICAL GENETICS    Volume: 56    Issue: 1    Pages: 112-115    Published: MAR 13 1995  
Times Cited: 102     References: 20     
Abstract: The 14 tumors reported in Rubinstein-Taybi syndrome since 1989, when added to the 22 previously reported, are beginning to show a pattern of neural and developmental tumors, especially of the head, which is malformed in the syndrome. Among the neoplasms were 12 of the nervous systems: 2 each of oligodendroglioma, medulloblastoma, neuroblastoma, and benign meningioma, a pheochromocytoma, and 3 other benign tumors; 2 of nasopharyngeal rhabdomyosarcoma; and 1 each of leiomyosarcoma, seminoma, and embryonal carcinoma. Among the other benign tumors were an odontoma, a choristoma, a dermoid cyst, and 2 pilomatrixomas. (C) 1995 Wiley-Liss, Inc.
Document Type: Article
Language: English
Reprint Address: MILLER, RW (reprint author), NCI, CLIN EPIDEMIOL BRANCH, EPN 400, BETHESDA, MD 20892 USA
Addresses:
1. UNIV CINCINNATI, AFFILIATED CTR DEV DISORDERS, CINCINNATI, OH USA
2. UNIV CINCINNATI, COLL MED, DEPT PEDIAT, CINCINNATI, OH USA
3. CHILDRENS HOSP, MED CTR, CINCINNATI, OH 45229 USA
Publisher: WILEY-LISS, DIV JOHN WILEY & SONS INC 605 THIRD AVE, NEW YORK, NY 10158-0012
Subject Category: Genetics & Heredity
IDS Number: QJ893
ISSN: 0148-7299
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