Norrie disease: Linkage analysis using a 4.2-kb RFLP detected by a human ornithine aminotransferase cDNA probe

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1975 • 33,059 citations

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1983 • 26,063 citations

Selection of Hybrids from Matings of Fibroblasts in vitro and Their Presumed Recombinants

1964 • 2,108 citations

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

1974 • 1,022 citations

Polymorphic DNA region adjacent to the 5' end of the human insulin gene.

1981 • 910 citations

Improved techniques for the induction of mammalian cell hybridization by polyethylene glycol

1976 • 542 citations

GENETICS OF HUMAN CELL LINES, IV. DNA-MEDIATED HERITABLE TRANSFORMATION OF A BIOCHEMICAL TRAIT

1962 • 493 citations

A strategy to reveal high-frequency RFLPs along the human X chromosome.

1984 • 361 citations

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

1984 • 296 citations

Characterisation of deletions which affect the expression of fetal globin genes in man

1979 • 269 citations

Application of Endonuclease Mapping to the Analysis and Prenatal Diagnosis of Thalassemias Caused by Globin-Gene Deletion

1978 • 207 citations

Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.

1979 • 183 citations

Ornithine-δ-transaminase in the rat I. Assay and some general properties

1963 • 166 citations

Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes.

1977 • 148 citations

Gyrate atrophy of the choroid and retina associated with hyperornithinaemia.

1974 • 141 citations

Molecular cloning of human ornithine aminotransferase mRNA.

1986 • 94 citations

Gamma thalassemia resulting from the deletion of a gamma-globin gene.

1983 • 91 citations

A model for restriction fragment length distributions.

1983 • 76 citations

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease

1986 • 75 citations

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

1985 • 71 citations

X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome

1985 • 54 citations

Ouabain as a selective agent in the isolation of somatic cell hybrids

1975 • 53 citations

Ocular and Biochemical Abnormalities in Gyrate Atrophy of the Choroid and Retina

1978 • 49 citations

Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2.

1987 • 48 citations

Choroideremia and gyrate atrophy of the choroid and retina

1965 • 48 citations

144: Gyrate atrofy of the choroid and retina and ornithine-ketoacid aminotransferase deficiency

1976 • 39 citations

Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes

1987 • 37 citations

Primary vitreoretinal dysplasia resembling Norrie's disease in a female: association with X autosome chromosomal translocation.

1986 • 37 citations

Ornithine ketoacid aminotransferase in the bovine eye.

1980 • 35 citations

Accurate and superaccurate gene mapping.

1985 • 26 citations

Assignment of a human beta-crystallin gene to 17cen-q23

1986 • 23 citations

Recombinational event between Norrie disease and DXS7 loci

1988 • 19 citations

The use of multiple restriction fragment length polymorphisms in prenatal risk estimation. I. X-linked diseases.

1985 • 6 citations