Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia

American Journal of Human Genetics

Volumn 79, Issue 5, 2006, Pages 965-972

  Feuk, Lars ^a   Kalervo, Aino ^g   Lipsanen Nyman, Marita ^h   Skaug, Jennifer ^a   Nakabayashi, Kazuhiko ^a   Finucane, Brenda ⁱ   Hartung, Danielle ^j   Innes, Micheil ^k   Kerem, Batsheva ^l   Nowaczyk, Małgorzata J ^m   Rivlin, Joseph ⁿ   Roberts, Wendy ^b   Senman, Lili ^b   Summers, Anne ^c   Szatmari, Peter ^m   Wong, Virginia ^o   Vincent, John B ^d,e   Zeesman, Susan ^m   Osborne, Lucy R ^f   Cardy, Janis Oram ^p   Kere, Juha ^g,q   Scherer, Stephen W ^a,b,f   Hannula Jouppi, Katariina ^g   more..

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c NORTH YORK GENERAL HOSPITAL   (Canada)

^d CENTRE FOR ADDICTION AND MENTAL HEALTH   (Canada)

^e UNIVERSITY OF TORONTO   (Canada)

^f UNIVERSITY OF TORONTO   (Canada)

^g UNIVERSITY OF HELSINKI   (Finland)

^h HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

ⁱ Elwyn   (United States)

^j CHILDREN'S MEMORIAL HOSPITAL   (United States)

^k ALBERTA CHILDREN'S HOSPITAL   (Canada)

^l HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^m MCMASTER UNIVERSITY   (Canada)

ⁿ CARMEL MEDICAL CENTER   (Israel)

^o UNIVERSITY OF HONG KONG   (Hong Kong)

^p UNIVERSITY OF WESTERN ONTARIO   (Canada)

^q KAROLINSKA INSTITUTE   (Sweden)

more..

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADOLESCENT; ADULT; ARTICLE; AUTISM; CHILD; CHROMOSOME 7; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; DEVELOPMENTAL VERBAL DYSPRAXIA; DYSPRAXIA; FOXP2 GENE; GENE; GENE DELETION; GENE EXPRESSION; GENE MUTATION; HEMIZYGOSITY; HUMAN; INHERITANCE; NUCLEOTIDE SEQUENCE; PATERNAL INHERITANCE; PHENOTYPE; PRIORITY JOURNAL; REAL TIME POLYMERASE CHAIN REACTION; SILVER RUSSELL SYNDROME; SPEECH DEVELOPMENT;

EID: 33751113031     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/508902     Document Type: Article

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