Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9-2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP)

By Herzfeld Thilo  

Neurogenetics, Vol. 10, Iss. 1, 2009-02 ,pp. : 59-64

Springer Publishing Company

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A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze family

By Delague Valérie   Bareil Corinne   Bouvagnet Patrice   Salem Nabiha   Chouery Eliane   Loiselet Jacques   Mégarbané André   Claustres Mireille  

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Maternal and Paternal Age are Jointly Associated with Childhood Autism in Jamaica

By Rahbar Mohammad  

Journal of Autism and Developmental Disorders, Vol. 42, Iss. 9, 2012-09 ,pp. : 1928-1938

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A typical migraine susceptibility region localizes to chromosome 1q31

By Lea Rod   Shepherd Graeme   Curtain Robert   Nyholt Dale   Quinlan Sharon   Brimage Peter   Griffiths Lyn  

Neurogenetics, Vol. 4, Iss. 1, 2002-03 ,pp. : 17-22

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Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype?

By Angkustsiri Kathleen   Goodlin-Jones Beth   Deprey Lesley   Brahmbhatt Khyati   Harris Susan   Simon Tony  

Journal of Autism and Developmental Disorders, Vol. 44, Iss. 4, 2014-04 ,pp. : 739-746

Springer Publishing Company

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