Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

Journal of Medical Genetics

Volumn 41, Issue 4, 2004, Pages 241-248

  Shaw Smith, C ^b   Redon, R ^a   Rickman, L ^b   Rio, M ^c   Willatt, L ^d   Fiegler, H ^a   Firth, H ^b   Sanlaville, D ^c   Winter, R ^e   Colleaux, L ^c   Bobrow, M ^b   Carter, N P ^a  

^a WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^b UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d ADDENBROOKE S HOSPITAL   (United Kingdom)

^e UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME IDENTIFICATION; CLINICAL FEATURE; CLONE; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL MALFORMATION; DNA MICROARRAY; FEMALE; GENETIC SCREENING; GENOME; HUMAN; HUMAN CELL; LEARNING DISORDER; MALE; MENTAL DEFICIENCY; MOLECULAR CLONING; PHENOTYPE; PRIORITY JOURNAL;

EID: 11144356173     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.2003.017731     Document Type: Article

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