Isolation and characterization of a candidate gene for Norrie disease

Molecular Cloning: A Laboratory Manual

2001 • 133,517 citations

Molecular cloning: A laboratory manual

1990 • 85,659 citations

DNA sequencing with chain-terminating inhibitors

1977 • 69,181 citations

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

1983 • 26,063 citations

Genomic sequencing.

1984 • 8,343 citations

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

1987 • 5,139 citations

Organization and Expression of Eucaryotic Split Genes Coding for Proteins

1981 • 4,730 citations

Molecular Genetics of Human Color Vision: The Genes Encoding Blue, Green, and Red Pigments

1986 • 1,702 citations

Recognition of protein coding regions in DNA sequences

1982 • 927 citations

Report of the committee on the genetic constitution of the X chromosome (Part 1 of 3)

1990 • 597 citations

Positional cloning: Let's not call it reverse anymore

1992 • 485 citations

The gene family encoding the mouse ribosomal protein L32 contains a uniquely expressed intron-containing gene and an unmutated processed gene

1984 • 381 citations

Yeast artificial chromosome libraries containing large inserts from mouse and human DNA.

1991 • 331 citations

A model for the separation of large DNA molecules by crossed field gel electrophoresis

1987 • 304 citations

Removal of repeated sequences from hybridisation probes

1985 • 293 citations

A 3.5 genome equivalent multi access YAC library: construction, characterisation, screening and storage

1990 • 221 citations

Human monoamine oxidase A and B genes map to xp11.23 and are deleted in a patient with norrie disease

1989 • 199 citations

Norrie's disease. A congenital progressive oculo-acoustico-cerebral degeneration.

1966 • 137 citations

Monoamine oxidase deficiency in males with an X chromosome deletion

1989 • 110 citations

U1 small nuclear RNA genes are located on human chromosome 1 and are expressed in mouse-human hybrid cells.

1983 • 84 citations

Causes of Blindness in Children: Twenty-Five Years' Experience of Danish Institutes for the Blind

2017 • 83 citations

CAUSES OF BLINDNESS IN CHILDREN

1927 • 81 citations

Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis

1985 • 80 citations

Report of the committee on the genetic constitution of the X chromosome (Part 1 of 7)

1991 • 79 citations

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

1986 • 75 citations

Norrie disease resulting from a gene deletion: clinical features and DNA studies.

1988 • 69 citations

Assignment of the human locus determining phosphoglycolate phosphatase (PGP) to chromosome 16

1980 • 60 citations

Microdeletion in the X-chromosome and prenatal diagnosis in a family with Norrie disease

1989 • 35 citations

Norrie disease gene is distinct from the monoamine oxidase genes.

1989 • 33 citations

Long-range physical mapping around the human steroid sulfatase locus

1990 • 25 citations

Recombinational event between Norrie disease and DXS7 loci

1988 • 19 citations

First demonstration of recombination between the gene for Norrie disease and probe L1.28

1988 • 9 citations

Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp

1992 • 5 citations