Development and successful clinical application of preimplantation genetic haplotyping for Herlitz junctional epidermolysis bullosa

British Journal of Dermatology

Volumn 162, Issue 6, 2010, Pages 1330-1336

  Fassihi, H ^a   Liu, L ^b   Renwick, P J ^b   Braude, P R ^b   McGrath, J A ^a  

^a GUY S HOSPITAL   (United Kingdom)

^b GUY'S AND ST THOMAS' NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

Blister; Embryo; Laminin 332; Prenatal diagnosis; Skin

Indexed keywords

LAMININ; LAMININ BETA3; UNCLASSIFIED DRUG;

ARTICLE; CHROMOSOME 1; DINUCLEOTIDE REPEAT; DNA DETERMINATION; DNA FLANKING REGION; EMBRYO; EPIDERMOLYSIS BULLOSA; GENE AMPLIFICATION; GENE MUTATION; GENETIC HETEROGENEITY; HAPLOTYPE; HETEROZYGOTE DETECTION; HUMAN; HUMAN CELL; HUMAN TISSUE; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RISK FACTOR; UMBILICAL CORD BLOOD;

CELL ADHESION MOLECULES; CHROMOSOMES, HUMAN, 1-3; EPIDERMOLYSIS BULLOSA, JUNCTIONAL; FEMALE; GENETIC MARKERS; HAPLOTYPES; HUMANS; POLYMERASE CHAIN REACTION; PREGNANCY; PREIMPLANTATION DIAGNOSIS;

EID: 77952699551     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2010.09701.x     Document Type: Article

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