Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: A multicenter study

Human Mutation

Volumn 30, Issue 7, 2009, Pages 1082-1092

  McMullan, Dominic J ^a   Bonin, Michael ^b   Hehir Kwa, Jayne Y ^c   De Vries, Bert B A ^c   Dufke, Andreas ^b   Rattenberry, Eleanor ^a   Steehouwer, Marloes ^c   Moruz, Luminita ^c   Pfundt, Rolph ^c   De Leeuw, Nicole ^c   Riess, Angelika ^b   Altug Teber, Özge ^b   Enders, Herbert ^b   Singer, Sylke ^b   Grasshoff, Ute ^b   Walter, Michael ^b   Walker, Judith M ^a   Lamb, Catherine V ^a   Davison, E Val ^a   Brueton, Louise ^a   Riess, Olaf ^b   Veltman, Joris A ^c   more..

^a BIRMINGHAM WOMEN S HOSPITAL   (United Kingdom)

^b UNIVERSITY OF TÜBINGEN   (Germany)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

CNV; Mental retardation; Molecular karyotyping

Indexed keywords

ARTICLE; CLINICAL FEATURE; CLINICAL PRACTICE; CLINICAL TRIAL; CONTROLLED STUDY; DNA FINGERPRINTING; FEMALE; HOMOZYGOSITY; HUMAN; KARYOTYPING; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; MULTICENTER STUDY; PHENOTYPIC VARIATION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

GENE DOSAGE; GENETIC VARIATION; HETEROZYGOTE; HUMANS; KARYOTYPING; MENTAL RETARDATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; REAGENT KITS, DIAGNOSTIC; UNIPARENTAL DISOMY;

EID: 67649667022     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.21015     Document Type: Article

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