Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21

Genomics

Volumn 41, Issue 1, 1997, Pages 93-99

  Bruford, E A ^a   Riise, R ^b   Teague, P W ^a   Porter, K ^a   Thomson, K L ^a   Moore, A T ^c   Jay, M ^c   Warburg, M ^d   Schinzel, A ^e   Tommerup, N ^f   Tornqvist, K ^g   Rosenberg, T ^h   Patton, M ⁱ   Mansfield, D C ^a   Wright, A F ^a  

^a WESTERN GENERAL HOSPITAL   (United Kingdom)

^b Central Hospital of Hedmark   (Norway)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d UNIVERSITY OF COPENHAGEN   (Denmark)

^e UNIVERSITY OF ZURICH   (Switzerland)

^f JOHN F KENNEDY INSTITUTE   (Denmark)

^g LUND UNIVERSITY HOSPITAL   (Sweden)

^h National Eye Clinic for the Visually Impaired Denmark   (Denmark)

ⁱ ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BARDET BIEDL SYNDROME; CHROMOSOME 11Q; CHROMOSOME 15Q; CHROMOSOME 16Q; CHROMOSOME SATELLITE; GENE LOCUS; GENETIC LINKAGE; GENOTYPE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; SCORING SYSTEM;

GENETTA;

EID: 0031127101     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.4613     Document Type: Article

References (25)

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