Finckh, U

Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3. [electronic resource] - Genomics Mar 1998 - 341-5 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0888-7543

10.1006/geno.1997.5194 doi


Chromosome Mapping
Chromosomes, Human, Pair 16
Consanguinity
Crystallins--genetics
Genes, Recessive
Genetic Linkage
Haplotypes
Homozygote
Humans
Microsatellite Repeats
Pedigree
Retinitis Pigmentosa--genetics
mu-Crystallins