scholarly article | Q13442814 |
P2093 | author name string | Ferrell RE | |
Gorin MB | |||
Hong HK | |||
P2860 | cites work | Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests | Q24559869 |
Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 | ||
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity | Q26778490 | ||
A simple salting out procedure for extracting DNA from human nucleated cells | Q27861086 | ||
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28 | Q28265989 | ||
Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene | Q28268699 | ||
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy | Q28268707 | ||
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination | Q29620848 | ||
On the molecular genetics of retinitis pigmentosa | Q34419320 | ||
A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes | Q35196927 | ||
Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa | Q35198587 | ||
Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14. | Q35199496 | ||
Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis | Q35247496 | ||
A cytological map of the human X chromosome--evidence for non-random recombination | Q35290589 | ||
PCR detection of existing and new polymorphism at the TIMP locus | Q40532077 | ||
X-linked progressive cone dystrophy. Clinical characteristics of affected males and female carriers | Q44224593 | ||
Report of the Committee on the Genetic Constitution of the X and Y Chromosomes | Q44429358 | ||
Two different genes for X-linked retinitis pigmentosa | Q45310086 | ||
Dinucleotide repeat polymorphism at the DXS1146 locus | Q48112475 | ||
Linkage between the X-linked retinitis pigmentosa locus and the L1.28 locus | Q49197535 | ||
Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3 | Q57971945 | ||
Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: Implications for norrie disease | Q60641504 | ||
Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7 | Q68519079 | ||
Color matching and foveal densitometry in patients and carriers of an X-linked progressive cone dystrophy | Q68629114 | ||
X-linked recessive cone dystrophy with tapetal-like sheen. A newly recognized entity with Mizuo-Nakamura phenomenon | Q68804982 | ||
Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers | Q69837442 | ||
X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome | Q70101111 | ||
A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens | Q70691294 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cone dystrophy | Q147270 |
P304 | page(s) | 1173-1181 | |
P577 | publication date | 1994-12-01 | |
P1433 | published in | American Journal of Human Genetics | Q4744249 |
P1476 | title | Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1) | |
P478 | volume | 55 |
Q24677020 | A new genetic locus for X linked progressive cone-rod dystrophy |
Q24538863 | Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. |
Q34384129 | Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3. |
Q35250459 | Localization of a novel X-linked progressive cone dystrophy gene to Xq27: evidence for genetic heterogeneity |
Q24305973 | X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene |
Q37216323 | X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15 |
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