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Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis and mental retardation, caused by deletions on the short arm of chromosome 11

Authors :
Bartsch, O.
wim wuyts
Wim Van Hul
Hecht, J. T.
Meinecke, P.
Hogue, D.
Werner, W.
Zabel, B.
Hinkel, G. K.
Powell, C. M.
Shaffer, L. G.
Willems, P.
Source :
The American journal of human genetics, University of Antwerp
Publication Year :
1996

Details

Language :
English
ISSN :
00029297
Database :
OpenAIRE
Journal :
The American journal of human genetics
Accession number :
edsair.dedup.wf.001..728e4bff17e99c3771cff72480d96ab7