Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175

Human Molecular Genetics

Volumn 5, Issue 1, 1996, Pages 169-173

  Brown, K A ^a   Janjua, A H ^b   Karbani, G ^c   Parry, G ^d   Noble, A ^a   Crockford, G ^c   Bishop, D T ^c   Newton, V E ^b   Markham, A F ^a   Mueller, R F ^c  

^a UNIVERSITY OF LEEDS   (United Kingdom)

^b UNIVERSITY OF MANCHESTER   (United Kingdom)

^c ST JAMES S UNIVERSITY HOSPITAL   (United Kingdom)

^d ST LUKE S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 13; CLINICAL ARTICLE; FAMILY STUDY; FEMALE; GENE MAPPING; GENETIC LINKAGE; GENETIC RECOMBINATION; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; MALE; MARKER GENE; PAKISTAN; PRIORITY JOURNAL;

CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 13; CONSANGUINITY; DEAFNESS; FEMALE; GENES, RECESSIVE; GENOTYPE; GREAT BRITAIN; HUMANS; LOD SCORE; MALE; PAKISTAN; PEDIGREE;

EID: 9044254521     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.1.169     Document Type: Article

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