PGD for dystrophin gene deletions using fluorescence in situ hybridization

Molecular Human Reproduction

Volumn 12, Issue 5, 2006, Pages 353-356

  Malmgren, H ^a   White, I ^a   Johansson, S ^b   Levkov, L ^b   Iwarsson, E ^a   Fridstrom M ^b   Blennow, Elisabeth ^a,b  

^a KAROLINSKA INSTITUTE   (Sweden)

^b KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Becker muscular dystrophy; Duchenne muscular dystrophy; Dystrophin gene; Fluorescence in situ hybridization; PGD

Indexed keywords

CHORIONIC GONADOTROPIN; DYSTROPHIN; PROGESTERONE; RECOMBINANT FOLLITROPIN;

ADULT; ARTICLE; BECKER MUSCULAR DYSTROPHY; BLASTOMERE; CASE REPORT; CENTROMERE; DIAGNOSTIC VALUE; DUCHENNE MUSCULAR DYSTROPHY; EMBRYO; EXON; FEMALE; FERTILIZATION IN VITRO; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MUTATION; HETEROZYGOTE; HUMAN; HUMAN TISSUE; INFERTILITY; MALE; OVULATION INDUCTION; POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SEX DETERMINATION;

ADULT; BLASTOMERES; DYSTROPHIN; EXONS; FEMALE; GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MUSCLE, SKELETAL; MUSCULAR DYSTROPHIES; MUSCULAR DYSTROPHY, DUCHENNE; PREGNANCY; PREIMPLANTATION DIAGNOSIS;

EID: 33744719087     PISSN: 13609947     EISSN: 14602407     Source Type: Journal    
DOI: 10.1093/molehr/gal039     Document Type: Article

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