A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22

By Ouled Amar Ben Cheikh Bouchra  

Neurogenetics, Vol. 10, Iss. 1, 2009-02 ,pp. : 35-42

Springer Publishing Company

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Additional evidence of a locus for complex febrile and afebrile seizures on chromosome 12q22-23.3

By Gurnett Christina   Dobbs Matthew   Keppel Catherine   Pincus Elisa   Jansen Laura   Bowcock Anne  

Neurogenetics, Vol. 8, Iss. 1, 2007-01 ,pp. : 61-63

Springer Publishing Company

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Novel locus for benign hereditary chorea with adult onset maps to chromosome 8q21.3–q23.3

By Shimohata Takayoshi  

Brain, Vol. 130, Iss. 9, 2007-09 ,pp. : 2302-2309

Oxford University Press

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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  

Neurogenetics, Vol. 4, Iss. 1, 2002-03 ,pp. : 23-27

Springer Publishing Company

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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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