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Chromosome deletion 17pl 1.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation.

Authors :
Behjati, F.
Mullarkey, M.
Bergbaum, A.
Berry, A. C.
Docherty, Z.
Source :
Clinical Genetics; Jan1997, Vol. 51 Issue 1, p71-74, 4p
Publication Year :
1997

Details

Language :
English
ISSN :
00099163
Volume :
51
Issue :
1
Database :
Complementary Index
Journal :
Clinical Genetics
Publication Type :
Academic Journal
Accession number :
62129356
Full Text :
https://doi.org/10.1111/j.1399-0004.1997.tb02420.x