Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

Developmental Medicine and Child Neurology

Volumn 56, Issue 4, 2014, Pages 346-353

  Simpson, Nuala H ^a   Addis, Laura ^b   Brandler, William M ^c   Slonims, Vicky ^d   Clark, Ann ^e   Watson, Jocelynne ^e   Scerri, Thomas S ^f   Hennessy, Elizabeth R ^g   Bolton, Patrick F ^b   Conti Ramsden, Gina ^h   Fairfax, Benjamin P ^a   Knight, Julian C ^a   Stein, John ^c   Talcott, Joel B ⁱ   O'Hare, Anne ^j   Baird, Gillian ^d   Paracchini, Silvia ^k   Fisher, Simon E ^l,m   Newbury, Dianne F ^a   Nudel, R ^a   Monaco, A P ^a   Simonoff, E ^b   Pickles, A ^b   Everitt, A ^g   Seckl, J ^j   Cowie, H ⁿ   Cohen, W ^o   Nasir, J ^p   Bishop, D V M ^c   Simkin, Z ^h   more..

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b KING'S COLLEGE LONDON   (United Kingdom)

^c UNIVERSITY OF OXFORD   (United Kingdom)

^d EVELINA LONDON CHILDREN S HOSPITAL   (United Kingdom)

^e QUEEN MARGARET UNIVERSITY   (United Kingdom)

^f WALTER AND ELIZA HALL INSTITUTE OF MEDICAL RESEARCH   (Australia)

^g UNIVERSITY OF ABERDEEN   (United Kingdom)

^h UNIVERSITY OF MANCHESTER   (United Kingdom)

ⁱ ASTON UNIVERSITY   (United Kingdom)

^j UNIVERSITY OF EDINBURGH   (United Kingdom)

^k UNIVERSITY OF ST ANDREWS   (United Kingdom)

^l MAX PLANCK INSTITUTE FOR PSYCHOLINGUISTICS   (Netherlands)

^m RADBOUD UNIVERSITY   (Netherlands)

ⁿ ROYAL HOSPITAL FOR SICK CHILDREN   (United Kingdom)

^o UNIVERSITY OF STRATHCLYDE   (United Kingdom)

^p ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

45,X/46,XY MOSAICISM; ADOLESCENT; ADULT; ARTICLE; CHILD; COHORT ANALYSIS; CONTROLLED STUDY; DYSLEXIA; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENOTYPE; HUMAN; KARYOTYPE 45,X; KARYOTYPE 47,XXX; KARYOTYPE 47,XXY; KARYOTYPE 47,XYY; KARYOTYPING; KLINEFELTER SYNDROME; LANGUAGE DELAY; LANGUAGE DISABILITY; MAJOR CLINICAL STUDY; MALE; POPULATION; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SEX CHROMOSOME ABERRATION; SINGLE NUCLEOTIDE POLYMORPHISM; SPEECH THERAPY; TURNER SYNDROME; YOUNG ADULT;

ADOLESCENT; ANEUPLOIDY; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; DYSLEXIA; FEMALE; GENOTYPE; HUMANS; KARYOTYPING; LANGUAGE DEVELOPMENT DISORDERS; MALE; PATERNAL AGE; POLYMORPHISM, SINGLE NUCLEOTIDE; PREVALENCE; SEX CHROMOSOMES; YOUNG ADULT;

EID: 84896102139     PISSN: 00121622     EISSN: 14698749     Source Type: Journal    
DOI: 10.1111/dmcn.12294     Document Type: Article

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