Linkage analysis in Usher syndrome type I (USH1) families from Spain

Journal of Medical Genetics

Volumn 35, Issue 5, 1998, Pages 391-398

  Espinós, Carmen ^a   Nájera, Carmen ^a   Millán, José Maria ^b   Ayuso, Carmen ^c   Baiget, Montserrat ^d   Pérez Garrigues, Herminio ^b   Rodrigo, Onofre ^b   Vilela, Concepción ^b   Beneyto, Magdalena ^a  

^a UNIVERSITY OF VALENCIA   (Spain)

^b HOSPITAL UNIVERSITARIO LA FE   (Spain)

^c Funda ción Jiménez Díaz   (Spain)

^d HOSPITAL DE LA SANTA CREU I SANT PAU   (Spain)

Author keywords

Genetic heterogeneity; Linkage analysis; Usher syndrome

Indexed keywords

DNA MARKER;

ADULT; ARTICLE; CHROMOSOME 11Q; CHROMOSOME 3Q; CLINICAL ARTICLE; FEMALE; GENETIC HETEROGENEITY; GENETIC LINKAGE; HUMAN; HUMAN CELL; MALE; PRIORITY JOURNAL; SPAIN; USHER SYNDROME;

EID: 0031945676     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.35.5.391     Document Type: Article

References (9)

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9. Wagenaar M, ter Rahe B, van Aarem A, et al. Clinical findings in obligate carriers of type I Usher syndrome. Am J Med Genet 1995;59:375-9.