A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1 [alpha]

Authors :: Zahir, F.R.
Baross, A.
Delaney, A.D.
Eydoux, P.
Fernandes, N.D.
Pugh, T.
Marra, M.A.
Friedman, J.M.
Source :: Journal of Medical Genetics. April, 2008, Vol. 45 Issue 4, p239, 5 p.
Publication Year :: 2008

Subjects :: Mental retardation -- Genetic aspects
Mental retardation -- Physiological aspects
Mental retardation -- Research
Chromosome deletion -- Analysis
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