Now showing items 141-150 of 184
Identification of new markers in Xp21 between DXS28 (C7) and DMD
(Elsevier, 1992-08)
Characterization of Xp21 distal to Duchenne muscular dystrophy (DMD) in the region containing the genes for adrenal hypoplasia congenita (AHC) and glycerol kinase deficiency (GKD) has been limited due to a paucity of probes. ...
The Genes Encoding Gonadal and Nongonadal Forms of 3[beta]-Hydroxysteroid Dehydrogenase/[Delta]5-[Delta]4 Isomerase Are Closely Linked on Mouse Chromosome 3
(Elsevier, 1993-04)
The biosynthesis of steroid hormones in the gonads and adrenal glands requires the activities of the enzyme 3[beta]-hydroxysteroid dehydrogenase/isomerase (3[beta]HSD) which catalyzes the NAD+-dependent dehydrogenation and ...
Commingling and segregation analyses: Comparison of results from a simulation study of a quantitative trait
(Wiley Subscription Services, Inc., A Wiley Company, 1990)
Commingling analysis is commonly used to provide preliminary evidence for a single genetic locus with a major effect on the quantitative trait of interest. In this paper, the effectiveness of commingling analysis as a ...
Problem of “false positive” conclusions in genetic epidemiology: Lessons from the leukemia cluster near the sellafield nuclear installation
(Wiley Subscription Services, Inc., A Wiley Company, 1994)
No Abstract.
Variation at the M235T locus of the angiotensinogen gene and essential hypertension: a population-based case-control study from Rochester, Minnesota
(Springer-Verlag, 1995-09)
A variant of the angiotensinogen gene, M235T, has been associated with essential hypertension in selected subjects from Paris, France and Salt Lake City, Utah. In the present report, we studied a population-based sample ...
A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locus
(Elsevier, 1992-11)
We describe a high-resolution radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 (NF2) gene. Eighty-five hamster--human somatic cell hybrids generated by X-irradiation and ...
Physical mapping of the nail patella syndrome interval at 9q34: ordering of STSs and ESTs
(Springer-Verlag; Springer-Verlag Berlin Heidelberg, 1998-11)
DXS165 detects a translocation breakpoint in a woman with choroideremia and a de novo X; 13 translocation
(Elsevier, 1990-04)
The search for the gene for choroideremia (MIM 30310), a rare retinal dystrophy, has been of great interest due to the existence of several choroideremia patients with well-defined structural chromosome aberrations, thus ...