WAGR syndrome and multiple exostoses in a patient with del (11) (p11.2p14.2)

McGaughran, JM, Ward, HB and Evans, Dgr (1995) WAGR syndrome and multiple exostoses in a patient with del (11) (p11.2p14.2). Journal of Medical Genetics, 32 10: 823-824. doi:10.1136/jmg.32.10.823


Author McGaughran, JM
Ward, HB
Evans, Dgr
Title WAGR syndrome and multiple exostoses in a patient with del (11) (p11.2p14.2)
Journal name Journal of Medical Genetics   Check publisher's open access policy
ISSN 0022-2593
Publication date 1995-01-01
Year available 1995
Sub-type Article (original research)
DOI 10.1136/jmg.32.10.823
Open Access Status Not yet assessed
Volume 32
Issue 10
Start page 823
End page 824
Total pages 2
Place of publication LONDON
Publisher BMJ Publishing Group
Language eng
Subject 2739 Public Health, Environmental and Occupational Health
3306 Health (social science)
1311 Genetics
2716 Genetics (clinical)
Abstract The WAGR syndrome (Wilms' tumour, aniridia, genital anomalies, and mental retardation) is well documented to be associated with a deletion of 11p13. We present a patient with a del(11)(p11.2p14.2) who as well as all the features of WAGR syndrome has multiple exostoses. We suggest that this could be a possible locus for hereditary multiple exostoses.
Keyword Genetics & Heredity
Genetics & Heredity
GENETICS & HEREDITY
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Unknown

Document type: Journal Article
Sub-type: Article (original research)
Collection: Scopus Import - Archived
 
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Citation counts: TR Web of Science Citation Count  Cited 22 times in Thomson Reuters Web of Science Article | Citations
Scopus Citation Count Cited 24 times in Scopus Article | Citations
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