Detection of turner syndrome using high-throughput quantitative genotyping

Journal of Clinical Endocrinology and Metabolism

Volumn 90, Issue 6, 2005, Pages 3419-3422

  Meng, Haiying ^a   Hager, Karl ^a   Rivkees, Scott A ^a   Gruen, Jeffrey R ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; ASSAY; DATA BASE; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; DISEASE MARKER; FEMALE; GENOTYPE; HIGH THROUGHPUT SCREENING; HUMAN; KARYOTYPE 45,X; KARYOTYPE 46,XX; KARYOTYPE 46,XY; MAJOR CLINICAL STUDY; MALE; MOSAICISM; NEWBORN SCREENING; PRIORITY JOURNAL; QUANTITATIVE GENETICS; SEX CHROMOSOME ABERRATION; SINGLE NUCLEOTIDE POLYMORPHISM; TURNER SYNDROME; X CHROMOSOME; Y CHROMOSOME; ZYGOSITY; GENETICS; KARYOTYPING; NOONAN SYNDROME;

CHROMOSOMES, HUMAN, X; CHROMOSOMES, HUMAN, Y; FEMALE; GENOTYPE; HUMANS; KARYOTYPING; MALE; NOONAN SYNDROME; TURNER SYNDROME;

EID: 21244470759     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.2005-0544     Document Type: Article

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