Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7

Genomics

Volumn 12, Issue 2, 1992, Pages 409-411

  Bech Hansen, N Torben ^a,b   Moore, Brenda J ^a,b   Pearce, William G ^a,b,c  

^a ALBERTA CHILDREN'S HOSPITAL   (Canada)

^b UNIVERSITY OF CALGARY   (Canada)

^c UNIVERSITY OF ALBERTA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME XP; GENE MAPPING; HUMAN; MALE; NIGHT BLINDNESS; X CHROMOSOMAL INHERITANCE;

ALLELES; CHROMOSOME MAPPING; FEMALE; HAPLOTYPES; HUMAN; LINKAGE (GENETICS); MALE; NIGHT BLINDNESS; PEDIGREE; SUPPORT, NON-U.S. GOV'T; X CHROMOSOME;

EID: 0026511032     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1016/0888-7543(92)90394-8     Document Type: Article

References (15)

1. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs
2. A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome
3. Congenital stationary night blindness
4. Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa
5. Identification and application of additional restriction fragment length polymorphisms at the human ornithine transcarbamylase locus
6. Multi-allelic RFLP for M27-beta an anonymous single copy genomic clone at Xp113-Xcen [HGM9 provisional No DXS255]
7. Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp
8. Report of the committee on linkage and gene order
9. A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: Linkage mapping of the synapsin I/A-raf-I genes
10. Five polymorphic microsatellite VNTRs on the human X chromosome
11. Report of the committee on the genetic constitution of the X chromosome
12. A polymorphic dinucleotide repeat at locus DXS7
13. Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3
14. Variable expressivity in X-linked congenital stationary night blindness