Case report: First successful application of preimplantation genetic diagnosis for hereditary angiooedema

Reproductive BioMedicine Online

Volumn 21, Issue 5, 2010, Pages 658-662

  Bautista Llácer, Rosa ^a   Alberola, Trinitat M ^a   Vendrell, Xavier ^a   Fernández, Esther ^b   Pérez Alonso, Manuel ^a  

^a Reproductive Genetics Unit   (Spain)

^b IVF Laboratory Quirón Madrid   (Spain)

Author keywords

haplotype analysis; hereditary angiooedema; molecular PGD; monogenic disease; preimplantation genetic diagnosis

Indexed keywords

ADULT; ALLELE; ANGIONEUROTIC EDEMA; ARTICLE; CASE REPORT; EMBRYO; EMBRYO TRANSFER; EXON; FEMALE; GENE; GENE LOCUS; GENETIC SCREENING; HAPLOTYPE; HUMAN; MULTIPLEX POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; SERPING1 GENE; SHORT TANDEM REPEAT;

ADULT; ANGIOEDEMAS, HEREDITARY; COMPLEMENT C1 INACTIVATOR PROTEINS; FEMALE; HUMANS; MALE; PEDIGREE; POLYMERASE CHAIN REACTION; PREGNANCY; PREIMPLANTATION DIAGNOSIS; SEQUENCE DELETION;

EID: 78049455142     PISSN: 14726483     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.rbmo.2010.05.016     Document Type: Article

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