Presence of large deletions in kindreds with autism

American Journal of Human Genetics

Volumn 71, Issue 1, 2002, Pages 100-115

  Yu, Chang En ^a,b   Dawson, Geraldine ^c   Munson, Jeffrey ^c   D'Souza, Ian ^a,b   Osterling, Julie ^c   Estes, Annette ^c   Leutenegger, Anne Louise ^d   Flodman, Pamela ^g   Smith, Moyra ^g   Raskind, Wendy H ^e   Spence, M Anne ^g   McMahon, William ^h   Wijsman, Ellen M ^d,e   Schellenberg, Gerard D ^a,b,f  

^a VETERANS AFFAIRS MEDICAL CENTER   (United States)

^b Division of Gerontology and Geriatric Medicine   (United States)

^c Center on Human Development and Disability   (United States)

^d Department of Biostatistics ^*  (United States)

^e Division of Medical Genetics   (United States)

^f UNIVERSITY OF WASHINGTON   (United States)

^g UNIVERSITY OF CALIFORNIA   (United States)

^h UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ALLELISM; ALZHEIMER DISEASE; ARTICLE; AUTISM; CHILD; CORRELATION ANALYSIS; DIAGNOSTIC VALUE; DISEASE ASSOCIATION; FEMALE; GENE DELETION; GENETIC MARKER; GENETIC POLYMORPHISM; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; HUMAN; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MALE; MARKER GENE; MEIOSIS; MULTIGENE FAMILY; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SCREENING TEST;

EID: 18444371140     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/341291     Document Type: Article

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