Analysis of three deletion breakpoints in Xp21.1 and the Further localization of RP3

Genomics

Volumn 37, Issue 2, 1996, Pages 200-210

  Brown, John ^a   Dry, Katherine L ^a   Edgar, Alexander J ^a   Pryde, Fiona E ^a   Hardwick, Lee J ^a   Aldred, Micheala A ^a   Lester, Douglas H ^a   Boyle, Shelagh ^a   Kaplan, Josseline ^c   Dufier, Jean Louis ^c   Ho, Meng Fatt ^d   Monaco, Anthony M ^d   Musarella, Maria A ^e   Wright, Alan F ^a,b  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b UNIVERSITY OF EDINBURGH   (United Kingdom)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d UNIVERSITY OF OXFORD   (United Kingdom)

^e HOSPITAL FOR SICK CHILDREN RESEARCH INSTITUTE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; DYSTROPHIN;

ARTICLE; CASE REPORT; CHROMOSOME DELETION X; CHROMOSOME XP; CHRONIC GRANULOMATOUS DISEASE; CONTROLLED STUDY; COSMID; DUCHENNE MUSCULAR DYSTROPHY; EXON; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE LOCATION; HUMAN; HUMAN CELL; HYPERTRANSLUCENT LUNG; INTRON; MALE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; SEQUENCE HOMOLOGY; TRANSPOSON;

EID: 0030588069     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0543     Document Type: Article

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