Live birth following the first mutation specific pre-implantation genetic diagnosis for haemophilia A

Thrombosis and Haemostasis

Volumn 95, Issue 2, 2006, Pages 373-379

  Michaelides, Katerina ^a   Tuddenham, Edward G D ^a   Turner, Cathy ^b   Lavender, Ben ^b   Lavery, Stuart A ^b  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

^b IVF Unit   (United Kingdom)

Author keywords

FVIII; Haemophilia A; Inherited bleeding disorder; Preimplantation genetic diagnosis

Indexed keywords

BLOOD CLOTTING FACTOR 8; POLYACRYLAMIDE; PROTEINASE K; WATER;

ADULT; ALLELE; AMPLICON; ARTICLE; BLASTOMERE; CONTROLLED STUDY; CYTOLYSIS; DISEASE SEVERITY; EMBRYO; EMBRYO TRANSFER; EXON; FAMILY HISTORY; FEMALE; FERTILIZATION IN VITRO; GENE LOCUS; GENE MUTATION; HEMOPHILIA A; HETEROZYGOSITY; HETEROZYGOTE; HUMAN; LYMPHOCYTE; MALE; NUCLEOTIDE SEQUENCE; OVULATION INDUCTION; POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SEX DETERMINATION; TREATMENT FAILURE; UTERUS; X CHROMOSOME LINKED DISORDER;

ADULT; DNA MUTATIONAL ANALYSIS; EMBRYO TRANSFER; FACTOR VIII; FAMILY HEALTH; FEMALE; HEMOPHILIA A; HUMANS; LIVE BIRTH; MUTATION; POLYMERASE CHAIN REACTION; PREGNANCY; PREIMPLANTATION DIAGNOSIS;

EID: 33645552865     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1160/TH05-08-0574     Document Type: Article

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