Single intragenic microsatellite preimplantation genetic diagnosis for cystic fibrosis provides positive allele identification of all CFTR genotypes for informative couples

Molecular Human Reproduction

Volumn 7, Issue 3, 2001, Pages 307-312

  Eftedal, I ^a,b   Schwartz, M ^a   Bendtsen, H ^a   Andersen, A N ^a   Ziebe, S ^a  

^a Rigshospitalet   (Denmark)

^b TRONDHEIM UNIVERSITY HOSPITAL   (Norway)

Author keywords

Allele dropout; CFTR; Fluorescent PCR; Polymorphic microsatellite marker; Preimplantation genetic diagnosis

Indexed keywords

BIOLOGICAL MARKER; MICROSATELLITE DNA; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ALLELE; ARTICLE; BIOPSY; BLASTOMERE; CHILD; CHROMOSOME 7; CONTROLLED STUDY; CYSTIC FIBROSIS; DISEASE CARRIER; DISEASE SEVERITY; EMBRYO; EMBRYO DEVELOPMENT; EMBRYO TRANSFER; FAMILY STUDY; FEMALE; FLUORESCENCE; GENE INSERTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC PROCEDURES; GENETIC SCREENING; GENOTYPE; HETEROZYGOTE DETECTION; HUMAN; HUMAN TISSUE; MALE; MONOGENIC DISORDER; PLOIDY; POLYMERASE CHAIN REACTION; PREIMPLANTATION EMBRYO; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

EID: 0035102452     PISSN: 13609947     EISSN: None     Source Type: Journal    
DOI: 10.1093/molehr/7.3.307     Document Type: Article

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