Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) array

American Journal of Medical Genetics, Part A

Volumn 146, Issue 18, 2008, Pages 2346-2354

  Newkirk, H L ^a   Bittel, D C ^a   Butler, M G ^a  

^a CHILDREN S MERCY HOSPITAL   (United States)

Author keywords

Genetic testing; Microsphere suspension assay; PWS; Single copy probes

Indexed keywords

BIOTIN; GENOMIC DNA; MICROSPHERE; NUCLEOTIDE; PHYCOERYTHRIN; POLYSTYRENE; STREPTAVIDIN;

ARTICLE; CHROMOSOME 15Q; CHROMOSOME 15Q11; CHROMOSOME 15Q12; CHROMOSOME 15Q13; CHROMOSOME 7P; CHROMOSOME 7P22.1; COMPARATIVE STUDY; CONTROLLED STUDY; FEMALE; FLOW CYTOMETRY; FLUORESCENCE; GENE LOCUS; GENE PROBE; GENE SEQUENCE; HUMAN; HYBRIDIZATION; PRADER WILLI SYNDROME; PRIORITY JOURNAL; QUANTITATIVE MICROSPHERE HYBRIDIZATION ARRAY; CHROMOSOME 15; CHROMOSOME DELETION; CHROMOSOME MAP; DNA PROBE; GENE DOSAGE; GENETICS; METHODOLOGY; NUCLEIC ACID HYBRIDIZATION; SENSITIVITY AND SPECIFICITY;

CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 15; DNA PROBES; GENE DOSAGE; HUMANS; MICROSPHERES; NUCLEIC ACID HYBRIDIZATION; PRADER-WILLI SYNDROME; SENSITIVITY AND SPECIFICITY;

EID: 51449098809     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32459     Document Type: Article

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