Linkage analysis in X-linked ocular albinism
- 30 April 1991
- Vol. 9 (4), 605-613
- https://doi.org/10.1016/0888-7543(91)90353-g
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Partial deletions of a sequence family (“DXS278”) and its physical linkage to steroid sulfatase as detected by pulsed-field gel electrophoresisGenomics, 1990
- Report of the committee on linkage and gene orderCytogenetic and Genome Research, 1989
- Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markersGenomics, 1987
- Isolation and characterization of DNA probes from the short arm of the human X chromosome that detect restriction fragment length polymorphismsGenome, 1987
- A new syndrome of anosmia, ichthyosis, hypogonadism, and various neurological manifestations with deficiency of steroid sulfatase and arylsulfatase CAnnals of Neurology, 1986
- Giant pigment granules in the retinal pigment epithelium of a fetus with X-linked ocular albinismOphthalmic Paediatrics and Genetics, 1983
- Detection of specific sequences among DNA fragments separated by gel electrophoresisJournal of Molecular Biology, 1975
- OCULAR ALBINISM AND XgThe Lancet, 1971
- OCULAR ALBINISM AND XgThe Lancet, 1969
- OCULAR ALBINISM AND XgThe Lancet, 1968