[COMPREHENSIVE DIAGNOSTICS IN PATIENTS WITH GENOTYPE 47,XXY KLINEFELTER SYNDROME].

Akbarova, G A

Akbarova, G A.

Klin Med (Mosk) ; 94(3): 235-8, 2016.

Article in Ru | MEDLINE | ID: mdl-27522732

Subject(s)

Cholesterol/blood; Klinefelter Syndrome; Luteinizing Hormone/blood; Mental Disorders; Mental Retardation, X-Linked; Receptors, Androgen/genetics; Triglycerides/blood; Adult; Azerbaijan/epidemiology; Cleft Palate/diagnosis; Cleft Palate/genetics; Glucose/metabolism; Humans; Klinefelter Syndrome/diagnosis; Klinefelter Syndrome/epidemiology; Klinefelter Syndrome/genetics; Klinefelter Syndrome/psychology; Male; Mental Disorders/diagnosis; Mental Disorders/genetics; Mental Retardation, X-Linked/diagnosis; Mental Retardation, X-Linked/genetics; Phenotype; Psychosexual Development/physiology; Sequence Analysis; Social Skills

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Collection: 01-internacional Database: MEDLINE Main subject: Triglycerides / Luteinizing Hormone / Receptors, Androgen / Cholesterol / Mental Retardation, X-Linked / Klinefelter Syndrome / Mental Disorders Type of study: Diagnostic_studies Limits: Adult / Humans / Male Country/Region as subject: Europa Language: Ru Journal: Klin Med (Mosk) Year: 2016 Document type: Article

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