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Resolution of the two loci for autosomal dominant aniridia, AN1 and AN2, to a single locus on chromosome 11p13

  • Published:1992-08 Issue:4 Volume:13 Page:925-930
  • ISSN:0888-7543
  • Container-title:Genomics
  • language:en
  • Short-container-title:Genomics

Author:

Lyons Leslie A.,Martha Aruna,Mintz-Hittner Helen A.,Saunders Grady F.,Ferrell Robert E.

Publisher

Elsevier BV

Subject

Genetics

Reference30 articles.

1. Rapid typing of apolipoprotein B DNA polymorphisms by DNA amplification;Boerwinkle;Atherosclerosis,1990

2. Discontinuous polyacrylamide gel electrophoresis of DNA fragments;Budowle,1990

3. Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11;Compton;Cell,1988

4. Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci;Davis;Science,1988

5. Autosomal dominant aniridia: Probable linkage to acid phosphatase-1 locus on chromosome 2;Ferrell,1980

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2. Crystalline lens alterations in congenital aniridia;Archivos de la Sociedad Española de Oftalmología (English Edition);2021-11

3. Alteraciones del cristalino en la aniridia congénita;Archivos de la Sociedad Española de Oftalmología;2021-11

4. The Malformed Eye;Lee's Ophthalmic Histopathology;2021

5. Identification of a novel frameshift mutation in PAX6 gene and the clinical management in an Asian Indian aniridia family;Indian Journal of Ophthalmology;2018
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