Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. | Eur J Hum Genet;21(4): 361-5, 2013 Apr. | MEDLINE

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Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.

Newbury, Dianne F; Mari, Francesca; Sadighi Akha, Elham; Macdermot, Kay D; Canitano, Roberto; Monaco, Anthony P; Taylor, Jenny C; Renieri, Alessandra; Fisher, Simon E; Knight, Samantha J L.

Eur J Hum Genet ; 21(4): 361-5, 2013 Apr.

Article in En | MEDLINE | ID: mdl-22909776

Subject(s)

Apraxias/genetics; Chromosomes, Human, Pair 16/genetics; Sequence Deletion; Humans

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apraxias / Chromosomes, Human, Pair 16 / Sequence Deletion Limits: Humans Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2013 Type: Article

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apraxias / Chromosomes, Human, Pair 16 / Sequence Deletion Limits: Humans Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2013 Type: Article