Choroideremia: close linkage to DXYS1 and DXYS12 demonstrated by segregation analysis and historical‐genealogical evidence

Clinical Genetics

Volumn 31, Issue 5, 1987, Pages 315-322

  Sankila, E M ^a,b   Chapelle, A DE LA ^a,b   Karna, J ^c   Forsius, H ^c   Frants, R ^d   Eriksson, A ^d  

^a UNIVERSITY OF HELSINKI   (Finland)

^b FOLKHÄLSAN INSTITUTE OF GENETICS   (Finland)

^c UNIVERSITY OF OULU   (Finland)

^d VU UNIVERSITY AMSTERDAM   (Netherlands)

Author keywords

Choroideremia; DXYS1; DXYS12; haplotype; Key words:; linkage disequilibrium; X chromosome

Indexed keywords

CHOROIDEREMIA; CLINICAL ARTICLE; CONGENITAL DISORDER; ETIOLOGY; GENE SEGREGATION; GENEALOGY; GENETIC ENGINEERING; GENETIC LINKAGE; GEOGRAPHIC DISTRIBUTION; HEREDITY; HUMAN; PEDIGREE; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; VISUAL SYSTEM;

ALLELES; CHOROID; EPIDEMIOLOGIC METHODS; FEMALE; FINLAND; GENE FREQUENCY; HUMAN; LINKAGE (GENETICS); MALE; PEDIGREE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; PREGNANCY; PRENATAL DIAGNOSIS; SUPPORT, NON-U.S. GOV'T; UVEAL DISEASES; X CHROMOSOME;

EID: 0023186311     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1987.tb02815.x     Document Type: Article

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