Single cell detection of inherited retinoblastoma predisposition

Prenatal Diagnosis

Volumn 19, Issue 13, 1999, Pages 1231-1236

  Sütterlin, Marc ^a,c   Sleiman, Patrick Abou ^a   Onadim, Zerrin ^b   Delhanty, Joy ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^c UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

Automated laser fluorescence (ALF); Cancer predisposition syndromes; Preimplantation genetic diagnosis (PGD); Retinoblastoma (RB); Single cell analysis

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CANCER SUSCEPTIBILITY; CONTROLLED STUDY; DNA FINGERPRINTING; FEMALE; FLUORESCENCE ANALYSIS; GENE LOCUS; GENE MUTATION; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; PEDIGREE ANALYSIS; POLYACRYLAMIDE GEL ELECTROPHORESIS; POLYMERASE CHAIN REACTION; PREIMPLANTATION EMBRYO; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RETINOBLASTOMA; SINGLE STRAND CONFORMATION POLYMORPHISM; TANDEM REPEAT; TUMOR SUPPRESSOR GENE;

DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; DNA MUTATIONAL ANALYSIS; EMBRYONIC DEVELOPMENT; FEMALE; HUMANS; MALE; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PREGNANCY; PREIMPLANTATION DIAGNOSIS; RETINAL NEOPLASMS; RETINOBLASTOMA;

EID: 0343775773     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199912)19:13<1231::AID-PD725>3.0.CO;2-X     Document Type: Article

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