Hum Genet. 1990 Apr;84(5):406-8.

A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome.

Bech-Hansen NT, Field LL, Schramm AM, Reedyk M, Craig IW, Fraser NJ, Pearce WG.

Source

Alberta Children's Hospital Research Center, Calgary, Canada.

Abstract

Linkage between X-linked congenital stationary night blindness (CSNB1) and seven markers on the X chromosome was investigated in a large four-generation Albertan kindred. We detected significant linkage between the CSNB1 locus and the locus DXS255 (maximum lod score = 6.73 at a recombination fraction of 6%; confidence interval of 1% to 18%), which anchors the CSNB1 locus to the proximal region near p11.22 on the short arm of the X chromosome.

PMID:: 1969841; [PubMed - indexed for MEDLINE]

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Research Support, Non-U.S. Gov't

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Genetic Markers

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Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7. [Genomics. 1992]
Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7.
Bech-Hansen NT, Moore BJ, Pearce WG. Genomics. 1992 Feb; 12(2):409-11.
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Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3.
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Cited by 7 PubMed Central articles

Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. [Am J Hum Genet. 1998]
Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.
Boycott KM, Pearce WG, Musarella MA, Weleber RG, Maybaum TA, Birch DG, Miyake Y, Young RS, Bech-Hansen NT. Am J Hum Genet. 1998 Apr; 62(4):865-75.
Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: demonstration of homozygosity. [Am J Hum Genet. 1993]
Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: demonstration of homozygosity.
Bech-Hansen NT, Pearce WG. Am J Hum Genet. 1993 Jan; 52(1):71-7.
Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB. [J Med Genet. 1994]
Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB.
Bergen AA, Kestelyn P, Leys M, Meire F. J Med Genet. 1994 Jul; 31(7):580-2.

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