Oligonucleotide arrays for high-resolution analysis of copy number alteration in mental retardation/multiple congenital anomalies

Genetics in Medicine

Volumn 9, Issue 9, 2007, Pages 617-625

  Shaikh, Tamim H ^a,b  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Chromosomal rearrangement; Copy number variation; Mental retardation; Multiple congenital anomalies; Oligonucleotide microarrays

Indexed keywords

OLIGONUCLEOTIDE;

CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE NUMBER; GENETIC DISORDER; HUMAN; KARYOTYPING; MENTAL DEFICIENCY; MICROARRAY ANALYSIS; REVIEW; TELOMERE;

ABNORMALITIES, MULTIPLE; CHILD; GENE DOSAGE; HUMANS; MENTAL RETARDATION; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 34548665266     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/GIM.0b013e318148bb81     Document Type: Review

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