Timing of diagnosis of 47,XXY and 48,XXYY: A survey of parent experiences

American Journal of Medical Genetics, Part A

Volumn 161, Issue 2, 2013, Pages 268-272

  Visootsak, Jeannie ^a   Ayari, Natalie ^b,c   Howell, Susan ^b,c   Lazarus, Joash ^a   Tartaglia, Nicole ^b,c  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b University of Colorado Denver and Children s Hospital Colorado   (United States)

^c CHILDREN S HOSPITAL COLORADO   (United States)

Author keywords

Delayed diagnosis; Medical support; Sex chromosomal aneuploidies

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; COHORT ANALYSIS; DEVELOPMENTAL DISORDER; EXPERIENCE; HEALTH SURVEY; HUMAN; KARYOTYPE; KARYOTYPE 47,XXY; KARYOTYPE 48,XXYY; MAJOR CLINICAL STUDY; MALE; MEDICAL SPECIALIST; PARENT; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SEX CHROMOSOME ABERRATION;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; DATA COLLECTION; DEVELOPMENTAL DISABILITIES; GENETIC TESTING; HUMANS; INFANT; INFANT, NEWBORN; KLINEFELTER SYNDROME; MALE; MIDDLE AGED; PARENTS; TIME FACTORS; YOUNG ADULT;

EID: 84872952774     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.35709     Document Type: Article

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