Clinical experience with preimplantation genetic diagnosis of cystic fibrosis (ΔF508)

Prenatal Diagnosis

Volumn 16, Issue 2, 1996, Pages 137-142

  Ao, Asangla ^a   Ray, Pierre ^a   Harper, Joyce ^b   Lesko, John ^c   Paraschos, Thanos ^a   Atkinson, Glenn ^a   Soussis, Iakovos ^a   Taylor, Debbie ^a   Handyside, Alan ^a   Hughes, Mark ^c,d   Winston, Robert M L ^a  

^a HAMMERSMITH HOSPITAL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

F508 mutation; Cystic fibrosis; In vitro fertilization; Preimplantation genetic diagnosis

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CLINICAL TRIAL; CYSTIC FIBROSIS; DELETION MUTANT; EMBRYO; FERTILIZATION IN VITRO; GENETIC ANALYSIS; HUMAN; HUMAN CELL; POLYMERASE CHAIN REACTION; PREIMPLANTATION EMBRYO; PRIORITY JOURNAL;

ADULT; BIOPSY; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EMBRYO TRANSFER; EMBRYONIC DEVELOPMENT; FEMALE; GENETIC SCREENING; HUMANS; INFANT, NEWBORN; MUTATION; POLYMERASE CHAIN REACTION; PREGNANCY; PREGNANCY OUTCOME; PRENATAL DIAGNOSIS; RETROSPECTIVE STUDIES;

EID: 13344284633     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199602)16:2<137::AID-PD824>3.0.CO;2-H     Document Type: Article

References (19)

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