Drygt tio år med preimplantatorisk genetisk diagnostik i Sverige. Ett alternativ vid stor risk att få barn med svåra ärftliga sjukdomar

Lakartidningen

Volumn 105, Issue 14, 2008, Pages 1008-1010

  Blennow, Elisabeth ^a   Hanson, Charles ^b   Fridström, Margareta ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CONGENITAL DISORDER; FEMALE; GENETIC DISORDER; GENETIC SCREENING; GENETICS; HEALTH CARE DELIVERY; HUMAN; MALE; PREGNANCY; PREGNANCY OUTCOME; PRENATAL DIAGNOSIS; RISK FACTOR;

CONGENITAL ABNORMALITIES; FEMALE; GENETIC DISEASES, INBORN; GENETIC SCREENING; HEALTH SERVICES ACCESSIBILITY; HUMANS; MALE; PREGNANCY; PREGNANCY OUTCOME; PREIMPLANTATION DIAGNOSIS; RISK FACTORS;

EID: 42649091116     PISSN: 00237205     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)