A familial contiguous gene deletion syndrome at Xp22.3...

American Journal of Medical Genetics Part A 2003 Vol. 122A; Iss. 2

A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD

Kym M. Boycott, Malcolm I. Parslow, Judith L. Ross, Ivan P. Miller, N. Torben Bech-Hansen, Patrick M. MacLeod
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Volume:
122A
Year:
2003
Language:
english
Pages:
9
DOI:
10.1002/ajmg.a.20231
File:
PDF, 279 KB
english, 2003
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