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

Author:

Sankila E.-M.,Chapelle A. DE LA,Karna J.,Forsius H.,Frants R.,Eriksson A.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference28 articles.

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2. Report of the committee on methods of linkage analysis and reporting;Conneally;Cytogenet. Cell Genet.,1985

3. Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms;Drayna;Proc. Natl. Acad. Sci. USA,1984

4. The genetic map of the human X-chromosome;Drayna;Science,1985

5. Population genetics of C4 with the use of complementary DNA probes;Edwards;Phil. Trans. R. Soc. Lond.,1984

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1. Choroideremia: from genetic and clinical phenotyping to gene therapy and future treatments;Therapeutic Advances in Ophthalmology;2018-01

2. Shades of gray: a comparison of linkage disequilibrium between Hutterites and Europeans;Genetic Epidemiology;2009-08-20

3. Deletion of the DXS165 locus in patients with classical Choroideremia;Clinical Genetics;2008-06-28

4. Human Genetic Variation and Disease;Encyclopedia of Molecular Cell Biology and Molecular Medicine;2006-09-15

5. Choroideremia;Molecular Genetics of Inherited Eye Disorders;1994-12

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