Affected Females in X-Linked Congenital Stationary Night Blindness
- 1 May 1992
- journal article
- case report
- Published by Elsevier in Ophthalmology
- Vol. 99 (5) , 747-752
- https://doi.org/10.1016/s0161-6420(92)31902-5
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- X-chromosomal erbliche Nachtblindheit: Erkennen von Überträgerinnen durch Segregationsanalyse mit gekoppelten DNA-MarkernKlinische Monatsblätter für Augenheilkunde, 1990
- A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosomeHuman Genetics, 1990
- Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3Genomics, 1989
- Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on XpHuman Genetics, 1989
- Carrier detection in typical and atypical X-linked agammaglobulinemiaThe Journal of Pediatrics, 1988
- SEX‐LINKED ESSENTIAL NYCTALOPIA IN A NORWEGIAN FAMILYActa Ophthalmologica, 1974
- Choroideremia in a female.BMJ, 1968
- Electroretinographic findings (including flicker) in carriers of congenital X-linked achromatopsiaDocumenta Ophthalmologica, 1964
- X‐CHROMOSOMAL OCULAR ALBINISM IN A DUTCH FAMILY*Annals of Human Genetics, 1956
- Beitrag zur Analyse des menschlichen ElektroretinogrammsOphthalmologica, 1952