X chromosome array-CGH for the identification of novel X-linked mental retardation genes

European Journal of Medical Genetics

Volumn 48, Issue 3, 2005, Pages 263-275

  Bauters, Marijke ^a   Van Esch, Hilde ^b   Marynen, Peter ^a   Froyen, Guy ^a  

^a DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^b UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Array CGH; Genomic copy number changes; Mental retardation; X chromosome

Indexed keywords

ARTICLE; CHROMOSOME NUMBER; CLINICAL ARTICLE; COGNITION; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; FEMALE; GENE DELETION; GENE DUPLICATION; GENOME; GENOTYPE; HUMAN; MALE; MENTAL DEFICIENCY; MICROSCOPY; MOLECULAR CLONING; PATIENT; PHENOTYPE; REPRODUCIBILITY; SCREENING; VALIDATION PROCESS; X CHROMOSOME; X CHROMOSOME LINKED DISORDER;

CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, X; DNA; FEMALE; GENE DOSAGE; HUMANS; MALE; MENTAL RETARDATION, X-LINKED; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; VARIATION (GENETICS);

EID: 23944447954     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2005.04.008     Document Type: Article

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