Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population

European Journal of Human Genetics

Volumn 10, Issue 7, 2002, Pages 406-412

  Howard, Heidi C ^a,b   Dubé, Marie Pierre ^a,b   Prévost, Claude ^c   Bouchard, Jean Pierre ^d   Mathieu, Jean ^c   Rouleau, Guy A ^a,b  

^a MONTREAL GENERAL HOSPITAL   (Canada)

^b RESEARCH INSTITUTE OF THE MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

^c Hôtel Dieu de Chicoutimi   (Canada)

^d LAVAL UNIVERSITY   (Canada)

Author keywords

ACCPN; Agenesis corpus callosum; Founder population; Linkage disequilibrium; Recombination analysis

Indexed keywords

CONNEXIN 36; EYE PROTEIN; GAP JUNCTION PROTEIN; MICROSATELLITE DNA;

ARTICLE; CANADA; CHROMOSOME 15; CHROMOSOME MAP; CONGENITAL MALFORMATION; CORPUS CALLOSUM; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENETICS; HAPLOTYPE; HUMAN; MALE; NUCLEOTIDE SEQUENCE; PEDIGREE; PERIPHERAL NEUROPATHY; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 15Q; COMORBIDITY; CONTROLLED STUDY; CORPUS CALLOSUM AGENESIS; FACE DYSMORPHIA; FRANCE; GENE MAPPING; GENETIC POLYMORPHISM; GENETIC RECOMBINATION; MAJOR CLINICAL STUDY; MARKER GENE; MENTAL DEFICIENCY; PRIORITY JOURNAL; SENSORIMOTOR NEUROPATHY;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 15; CONNEXINS; CORPUS CALLOSUM; DNA MUTATIONAL ANALYSIS; EYE PROTEINS; FEMALE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MICROSATELLITE REPEATS; PEDIGREE; PERIPHERAL NERVOUS SYSTEM DISEASES; QUEBEC;

EID: 0036053506     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200815     Document Type: Article

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