48,XXYY, 48,XXXY and 49,XXXXY syndromes: Not just variants of Klinefelter syndrome

Acta Paediatrica, International Journal of Paediatrics

Volumn 100, Issue 6, 2011, Pages 851-860

  Tartaglia, Nicole ^a,b   Ayari, Natalie ^a   Howell, Susan ^a   D'Epagnier, Cheryl ^a   Zeitler, Philip ^a  

^a Children's Hospital Colorado   (United States)

^b CHILDREN S HOSPITAL COLORADO   (United States)

Author keywords

Hypogonadism; Klinefelter syndrome; XXXXY syndrome; XXXY syndrome; XXYY syndrome

Indexed keywords

FOLLITROPIN; LUTEINIZING HORMONE; TESTOSTERONE;

ANDROGEN DEFICIENCY; BEHAVIOR DISORDER; COGNITIVE DEFECT; CONGENITAL MALFORMATION; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HEREDITY; HUMAN; HYPOGONADISM; KARYOTYPE 48,XXXXY; KARYOTYPE 48,XXXY; KARYOTYPE 48,XXYY; KLINEFELTER SYNDROME; MALE INFERTILITY; PREPUBERTY; PRIORITY JOURNAL; REVIEW; SEX CHROMOSOME ABERRATION; SOCIAL ADAPTATION; SOCIAL EVOLUTION;

HUMANS; HYPOGONADISM; KLINEFELTER SYNDROME; MALE; PHENOTYPE; SEX CHROMOSOME DISORDERS; SYNDROME;

EID: 79955524495     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1111/j.1651-2227.2011.02235.x     Document Type: Review

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