Genetic and physical mapping of Xq24–q26 markers flanking the Lowe oculocerebrorenal syndrome
Open Access
- 1 September 1990
- Vol. 8 (1) , 62-70
- https://doi.org/10.1016/0888-7543(90)90226-k
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- MRI Findings and Peripheral Neuropathy in Lowe's SyndromeNeuropediatrics, 1988
- Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophyCytogenetic and Genome Research, 1988
- A genetic linkage map of the human genomeCell, 1987
- Lenticular Opacities in Carriers of Lowe's SyndromeOphthalmology, 1986
- Electrophoretic Separations of Large DNA Molecules by Periodic Inversion of the Electric FieldScience, 1986
- A balanced de novo X/autosome translocation in a girl with manifestations of lowe syndromeAmerican Journal of Medical Genetics, 1986
- A cytological map of the human X chromosome - evidence for non-random recombinationNucleic Acids Research, 1984
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983
- Arthropathy of Lowe's (Oculocerebrorenal) SyndromeArthritis & Rheumatism, 1983
- Oculo-Cerebro-Renal SyndromeAmerican Journal of Diseases of Children, 1968