A 47, XXY patient and Xq21.31 duplication with features of Prader-Willi syndrome: Results of array-based comparative genomic hybridization

Endocrine

Volumn 37, Issue 3, 2010, Pages 379-382

  Pramyothin, Pornpoj ^a   Pithukpakorn, Manop ^b   Arakaki, Richard F ^a  

^a UNIVERSITY OF HAWAII   (United States)

^b MAHIDOL UNIVERSITY   (Thailand)

Author keywords

DNA microarrays; Klinefelter syndrome; Prader Willi like syndrome; Xq duplication

Indexed keywords

FOLLITROPIN; FRAGILE X MENTAL RETARDATION PROTEIN; HEMOGLOBIN A1C; INSULIN; INSULIN SENSITIZING AGENT; LUTEINIZING HORMONE; TESTOSTERONE;

ADULT; ARTICLE; BODY HEIGHT; BODY MASS; BODY WEIGHT; CASE REPORT; CHROMOSOME DUPLICATION; CHROMOSOME XQ; COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISORDER; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE; HOMOZYGOSITY; HUMAN; HYPERGLYCEMIA; HYPOGONADISM; KARYOTYPE 47,XXY; KLINEFELTER SYNDROME; MALE; MICROPENIS; MORBID OBESITY; NON INSULIN DEPENDENT DIABETES MELLITUS; PHENOTYPE; POLYMERASE CHAIN REACTION; PRADER WILLI SYNDROME; PRIORITY JOURNAL;

EID: 77952098959     PISSN: 1355008X     EISSN: 15590100     Source Type: Journal    
DOI: 10.1007/s12020-010-9330-8     Document Type: Article

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