Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3

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

1983 • 26,063 citations

Improved technique utilizing nonfat dry milk for analysis of proteins and nucleic acids transferred to nitrocellulose

1984 • 1,697 citations

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

1974 • 1,022 citations

Congenital Stationary Night Blindness With Negative Electroretinogram

1986 • 439 citations

Report of the committee on methods of linkage analysis and reporting

1985 • 325 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

Beitrag zur Analyse des menschlichen Elektroretinogramms

1952 • 283 citations

Regional localization on the human X of DNA segments cloned from flow sorted chromosomes

1982 • 191 citations

X-Linked Ocular Albinism

1976 • 173 citations

The photopic electroretinogram in congenital stationary night blindness with myopia.

1983 • 122 citations

Loss of Electroretinographic Oscillatory Potentials, Optic Atrophy, and Dysplasia in Congenital Stationary Night Blindness

1983 • 94 citations

39 Congenital Stationary Night Blindness

2020 • 83 citations

Congenital stationary night blindness

1977 • 73 citations

A°land Island Eye Disease (Forsius-Eriksson Syndrome) Associated With Contiguous Deletion Syndrome at Xp21

1989 • 71 citations

A primary genetic map of the pericentromeric region of the human X chromosome

1988 • 59 citations

An electrophysiological and psychophysical study of two forms of congenital night blindness.

1969 • 58 citations

Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome

1985 • 55 citations

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp

1989 • 47 citations

Cone Electroretinograms in Congenital Nyctalopia with Myopia

1974 • 42 citations

X-linked Congenital Stationary Night Blindness

1988 • 41 citations

Åland eye disease: no albino misrouting

1985 • 38 citations

Forsius‐Eriksson syndrome: Its relation to the Nettleship‐Falls X‐linked ocular albinism

1980 • 36 citations

Syndrome of Congenital High Myopia with Nyctalopia

1970 • 35 citations

Åland Island eye disease (Forsius‐Eriksson ocular albinism) and an Xp21 deletion in a patient with duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasia

1990 • 35 citations

Reduced Amplitude of Oscillatory Potentials in Female Carriers of X-Linked Recessive Congenital Stationary Night Blindness

1984 • 32 citations

Congenital Stationary Night Blindness

2012 • 29 citations

ERG in a Case of X-Chromosomal Pigment Deficiency of Fundus in Combination with Myopia, Dyschromatopsia and Defective Dark-Adaptation *

2015 • 12 citations

Oscillatory potentials of X-linked carriers of congenital stationary night blindness.

1989 • 12 citations

Linkage and crossing-over in the human sen chromosomes

1940 • 11 citations

A New Pedigree of Idiopathic Congenital Night-Blindness* *From the Ophthalmological Clinic, University of Ghent (Director: Prof. François).

1965 • 11 citations

Ophthalmologic and Genetic Study of a Family with Nyctalopia and Myopia

1975 • 7 citations