Barriers to diagnosis of a rare neurological disorder in China-Lived experiences of Rett syndrome families

American Journal of Medical Genetics, Part A

Volumn 158 A, Issue 1, 2012, Pages 1-9

  Lim, Faye ^a   Downs, Jenny ^a,b   Li, Jianghong ^a,b   Bao, Xin Hua ^c   Leonard, Helen ^a  

^a UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^b CURTIN UNIVERSITY   (Australia)

^c PEKING UNIVERSITY FIRST HOSPITAL   (China)

Author keywords

China; Developing countries; Diagnosis; Qualitative research; Rett syndrome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHINA; CLINICAL ARTICLE; CONSULTATION; CULTURAL ANTHROPOLOGY; DIAGNOSTIC TEST; EXPERT SYSTEM; EXPLORATORY RESEARCH; FAMILY COUNSELING; FEMALE; HOSPITAL PLANNING; HOSPITAL SERVICE; HUMAN; INTERVIEW; KNOWLEDGE; MALE; NEUROLOGIC DISEASE; PERSONAL EXPERIENCE; PRACTICE GUIDELINE; PRIORITY JOURNAL; QUALITATIVE RESEARCH; RARE DISEASE; RETT SYNDROME;

CHINA; FEMALE; GENETIC COUNSELING; GENETIC TESTING; HUMANS; INFORMATION DISSEMINATION; MUTATION; QUESTIONNAIRES; RARE DISEASES; REFERRAL AND CONSULTATION; RETT SYNDROME;

EID: 84355166479     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34351     Document Type: Article

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