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Literature DB >> 5832305

Choroido-retinal dystrophy.

G W Hoare.

Abstract

Entities: Disease

Mesh：

Year: 1965 PMID： 5832305 PMCID： PMC506141 DOI： 10.1136/bjo.49.9.449

Source DB: PubMed Journal: Br J Ophthalmol ISSN： 0007-1161 Impact factor: 4.638

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4 in total

1. Chorioretinal heredo-degeneration.

Authors: J FRANCOIS
Journal: Proc R Soc Med Date: 1961-12

2. Dominant macular dystrophy.

Authors: A SORSBY; J B DAVEY
Journal: Br J Ophthalmol Date: 1955-07 Impact factor: 4.638

3. Choroideremia; clinical and genetic aspects.

Authors: A SORSBY; A FRANCESCHETTI; R JOSEPH; J B DAVEY
Journal: Br J Ophthalmol Date: 1952-10 Impact factor: 4.638

4. A sex-linked blood group.

Authors: J D MANN; A CAHAN; A G GELB; N FISHER; J HAMPER; P TIPPETT; R SANGER; R R RACE
Journal: Lancet Date: 1962-01-06 Impact factor: 79.321

4 in total

8 in total

1. Difference between RP2 and RP3 phenotypes in X linked retinitis pigmentosa.

Authors: C J Flaxel; M Jay; D L Thiselton; M Nayudu; A J Hardcastle; A Wright; A C Bird
Journal: Br J Ophthalmol Date: 1999-10 Impact factor: 4.638

2. Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.

Authors: A F Wright; S S Bhattacharya; M A Aldred; M Jay; A D Carothers; N S Thomas; A C Bird; B Jay; H J Evans
Journal: J Med Genet Date: 1991-07 Impact factor: 6.318

3. Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers.

Authors: R L Nussbaum; R A Lewis; J G Lesko; R Ferrell
Journal: Hum Genet Date: 1985 Impact factor: 4.132

Choroido-retinal dystrophy.

1. Chorioretinal heredo-degeneration.

2. Dominant macular dystrophy.

3. Choroideremia; clinical and genetic aspects.

4. A sex-linked blood group.

1. Difference between RP2 and RP3 phenotypes in X linked retinitis pigmentosa.

2. Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.

3. Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers.

4. Choroideremia in a female.

5. A genetic linkage study of a kindred with X-linked retinitis pigmentosa.

6. On the heredity of retinitis pigmentosa.

7. X-chromosomal-linked diseases affecting the eye: status of the heterozygote female.

8. Long-term follow-up of a family with dominant X-linked retinitis pigmentosa.