Genome wide analysis in a family with sensorineural hearing loss, autism and mental retardation

Gene

Volumn 510, Issue 2, 2012, Pages 102-106

  Mosrati, Mohamed Ali ^a   Schrauwen, Isabelle ^b   Kamoun, Hassen ^c   Charfeddine, Ilhem ^d   Fransen, Erik ^b   Ghorbel, Abdelmonem ^d   Van Camp, Guy ^b   Masmoudi, Saber ^a  

^a CENTRE DE BIOTECHNOLOGIE DE SFAX   (Tunisia)

^b UNIVERSITY OF ANTWERP   (Belgium)

^c UNIVERSITY OF SFAX   (Tunisia)

^d NONE   (Tunisia)

Author keywords

Autism; Candidate gene; Hearing loss; Linkage; Mental retardation

Indexed keywords

ADULT; ARTICLE; AUTISM; CHROMOSOME 6P; CHROMOSOME 7Q; CHROMOSOME 8P; CHROMOSOME DELETION; CLINICAL ARTICLE; CONGENITAL DEAFNESS; CONSANGUINITY; GENE CLUSTER; GENETIC ASSOCIATION; HUMAN; MENTAL DEFICIENCY; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; TUNISIA;

AUTISTIC DISORDER; CHROMOSOMES, HUMAN, PAIR 6; CHROMOSOMES, HUMAN, PAIR 7; CHROMOSOMES, HUMAN, PAIR 8; CONSANGUINITY; FEMALE; GENOME-WIDE ASSOCIATION STUDY; HEARING LOSS; HUMANS; INTELLECTUAL DISABILITY; MALE; MONOSOMY; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; TUNISIA;

EID: 84867336539     PISSN: 03781119     EISSN: 18790038     Source Type: Journal    
DOI: 10.1016/j.gene.2012.09.006     Document Type: Article

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