Diagnosis and mortality in 47,XYY persons: A registry study

Orphanet Journal of Rare Diseases

Volumn 5, Issue 1, 2010, Pages

  Stochholm, Kirstine ^a   Juul, Svend ^b   Gravholt, Claus H ^a  

^a AARHUS UNIVERSITY HOSPITAL   (Denmark)

^b AARHUS UNIVERSITY   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGE; AGED; ARTICLE; CAUSE OF DEATH; CHILD; CONTROLLED STUDY; DELAYED DIAGNOSIS; DENMARK; DIAGNOSIS; DISEASE REGISTRY; EPIDEMIOLOGICAL DATA; HUMAN; INJURY; INTERNATIONAL CLASSIFICATION OF DISEASES; KARYOTYPE; KARYOTYPE 47,XXY; LIFE EXPECTANCY; LIFESPAN; LUNG DISEASE; MAJOR CLINICAL STUDY; MALE; MORTALITY; NEOPLASM; NEUROLOGIC DISEASE; PRESCHOOL CHILD; PREVALENCE; SCHOOL CHILD; AGE DISTRIBUTION; GENETICS; KARYOTYPING; MULTIPLE MALFORMATION SYNDROME; REGISTER; SEX CHROMOSOME ABERRATION;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; AGE DISTRIBUTION; CHILD; CHILD, PRESCHOOL; HUMANS; KARYOTYPING; MALE; PREVALENCE; REGISTRIES; SEX CHROMOSOME ABERRATIONS; YOUNG ADULT;

EID: 77952695103     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-5-15     Document Type: Article

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