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American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 105, Issue 8, 2001, Pages 729-736

A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: Molecular analysis of the chromosome 7 breakpoint

(9) Tentler, Dmitry a,e Brandberg, Göran a,d,e Betancur, Catalina a,c,d,e Gillberg, Christopher a,d,e Annerén, Göran a,c,d,e Orsmark, Christina a,b,e Green, Eric D a,b,e Carlsson, Birgit a,b,e Dahl, Niklas a,b,c,d,e

a UPPSALA UNIVERSITY (Sweden)

b FALUN HOSPITAL (Sweden)

c FACULTÉ DE MÉDECINE (France)

d SAHLGRENSKA UNIVERSITY HOSPITAL (Sweden)

e NATIONAL HUMAN GENOME RESEARCH INSTITUTE (United States)

Author keywords

7q31 q32; Autism; Balanced reciprocal translocation; Breakpoint mapping

Indexed keywords

DNA;

ALLELE; ARTICLE; AUTISM; CASE REPORT; CHROMOSOME 7Q; CHROMOSOME TRANSLOCATION 5; DISEASE ASSOCIATION; DNA SEQUENCE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HUMAN; ONSET AGE; PREDICTION; PRIORITY JOURNAL; SCHOOL CHILD; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; SOUTHERN BLOTTING; SSBP GENE; T2R3 GENE;

AUTISTIC DISORDER; CHILD; CHROMOSOME BREAKAGE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 5; CHROMOSOMES, HUMAN, PAIR 7; DNA; DNA METHYLATION; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MICROSATELLITE REPEATS; MUTATION; TRANSLOCATION, GENETIC;

EID: 0035829982 PISSN: 15524841 EISSN: 1552485X Source Type: Journal
DOI: 10.1002/ajmg.1607 Document Type: Article

Times cited : (22)

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