DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation

Neurology

Volumn 68, Issue 10, 2007, Pages 743-750

  Engels, H ^a   Brockschmidt, A ^a   Hoischen, A ^a   Landwehr, C ^a   Bosse, K ^a   Walldorf, C ^a   Toedt, G ^b   Radlwimmer, B ^b   Propping, P ^a   Lichter, P ^b   Weber, R G ^a  

^a UNIVERSITY OF BONN   (Germany)

^b GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN MALFORMATION; CHILD; CHROMOSOME 22Q; CHROMOSOME ANALYSIS; CHROMOSOME BAND; CHROMOSOME DUPLICATION; CHROMOSOME XQ; COMPARATIVE GENOMIC HYBRIDIZATION; DNA DETERMINATION; DNA MICROARRAY; FACE DYSMORPHIA; FACIES; FEMALE; GENE DELETION; GENE IDENTIFICATION; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GROWTH RETARDATION; HUMAN; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; MICROCEPHALY; NEUROLOGIC DISEASE; PHENOTYPE; POPULATION RESEARCH; PRIORITY JOURNAL; SIBLING; CHROMOSOME ABERRATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION PROFILING; GENETICS; INFANT; METHODOLOGY; MULTIPLE MALFORMATION SYNDROME; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGY;

ABNORMALITIES, MULTIPLE; CHILD; CHROMOSOME ABERRATIONS; FEMALE; GENE EXPRESSION PROFILING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MAGNETIC RESONANCE IMAGING; MALE; MENTAL RETARDATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS;

EID: 33947495227     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000256367.70365.e0     Document Type: Article

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