Homozygosity Mapping of the Achromatopsia Locus in the Pingelapese
- 1 June 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (6) , 1679-1685
- https://doi.org/10.1086/302423
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- New Aspects of an Old Theme: The Genetic Basis of Human Color VisionAmerican Journal of Human Genetics, 1998
- Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in RecombinationAmerican Journal of Human Genetics, 1998
- Human Rod Monochromacy: Linkage Analysis and Mapping of a Cone Photoreceptor Expressed Candidate Gene on Chromosome 2q11Genomics, 1998
- Homozygosity and Linkage-Disequilibrium Mapping of the Syndrome of Congenital Hypoparathyroidism, Growth and Mental Retardation, and Dysmorphism to a 1-cM Interval on Chromosome 1q42-43American Journal of Human Genetics, 1998
- Linkage of Infantile Bartter Syndrome with Sensorineural Deafness to Chromosome 1pAmerican Journal of Human Genetics, 1998
- Homozygosity and Linkage‐Disequilibrium Mapping of the Urofacial (Ochoa) Syndrome Gene to a 1‐cM Interval on Chromosome 10q23‐q24American Journal of Human Genetics, 1997
- A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman IslandsHuman Molecular Genetics, 1996
- Novel approaches to linkage mappingCurrent Opinion in Genetics & Development, 1995
- Molecular Genetics of Human Blue Cone MonochromacyScience, 1989
- HEREDITARY BLINDNESS AMONG PINGELAPESE PEOPLE OF EASTERN CAROLINE ISLANDSThe Lancet, 1970