Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).

scientific article published in December 1994

Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1). is …
instance of (P31):
scholarly articleQ13442814

External links are
P932PMC publication ID1918428
P698PubMed publication ID7977377

P2093author name stringFerrell RE
Gorin MB
Hong HK
P2860cites workLocalizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity testsQ24559869
Detection of specific sequences among DNA fragments separated by gel electrophoresisQ25939003
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityQ26778490
A simple salting out procedure for extracting DNA from human nucleated cellsQ27861086
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28Q28265989
Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS geneQ28268699
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophyQ28268707
Multilocus linkage analysis in humans: detection of linkage and estimation of recombinationQ29620848
On the molecular genetics of retinitis pigmentosaQ34419320
A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genesQ35196927
Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosaQ35198587
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 analysisQ35247496
A cytological map of the human X chromosome--evidence for non-random recombinationQ35290589
PCR detection of existing and new polymorphism at the TIMP locusQ40532077
X-linked progressive cone dystrophy. Clinical characteristics of affected males and female carriersQ44224593
Report of the Committee on the Genetic Constitution of the X and Y ChromosomesQ44429358
Two different genes for X-linked retinitis pigmentosaQ45310086
Dinucleotide repeat polymorphism at the DXS1146 locusQ48112475
Linkage between the X-linked retinitis pigmentosa locus and the L1.28 locusQ49197535
Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3Q57971945
Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: Implications for norrie diseaseQ60641504
Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7Q68519079
Color matching and foveal densitometry in patients and carriers of an X-linked progressive cone dystrophyQ68629114
X-linked recessive cone dystrophy with tapetal-like sheen. A newly recognized entity with Mizuo-Nakamura phenomenonQ68804982
Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markersQ69837442
X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosomeQ70101111
A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescensQ70691294
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectcone dystrophyQ147270
P304page(s)1173-1181
P577publication date1994-12-01
P1433published inAmerican Journal of Human GeneticsQ4744249
P1476titleClinical diversity and chromosomal localization of X-linked cone dystrophy (COD1)
P478volume55

Reverse relations

cites work (P2860)
Q24677020A new genetic locus for X linked progressive cone-rod dystrophy
Q24538863Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.
Q34384129Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3.
Q35250459Localization of a novel X-linked progressive cone dystrophy gene to Xq27: evidence for genetic heterogeneity
Q24305973X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene
Q37216323X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15

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