Nance-Horan syndrome: Linkage analysis in 4 families refines localization in Xp22.31-p22.13 region

Human Genetics

Volumn 99, Issue 2, 1997, Pages 256-261

  Toutain, Annick ^a   Ronce, Nathalie ^a   Dessay, Benoît ^a   Robb, Laura ^b   Francannet, Christine ^c   Le Merrer, Martine ^d   Briard, Marie Louise ^d   Kaplan, Josseline ^d   Moraine, Claude ^a  

^a CHU BRETONNEAU   (France)

^b MONTREAL CHILDREN S HOSPITAL   (Canada)

^c HÔTEL DIEU   (France)

^d HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME XP; CLINICAL ARTICLE; CONGENITAL CATARACT; FACE MALFORMATION; GENE LOCATION; GENE MUTATION; GENE REARRANGEMENT; GENETIC LINKAGE; HAPLOTYPE; HUMAN; HUMAN CELL; MALE; PHENOTYPE; PRIORITY JOURNAL; TOOTH MALFORMATION;

ABNORMALITIES, MULTIPLE; ANIMALS; CATARACT; CHROMOSOME MAPPING; FEMALE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MICE; PEDIGREE; SYNDROME; TOOTH ABNORMALITIES; X CHROMOSOME;

EID: 0031033696     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050349     Document Type: Article

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