Identification of new markers in Xp21 between DXS28 (C7) and DMD
- 31 August 1992
- Vol. 13 (4) , 957-961
- https://doi.org/10.1016/0888-7543(92)90007-f
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Report of the committee on the genetic constitution of the X chromosome (Part 1 of 7)Cytogenetic and Genome Research, 1991
- Physical mapping distal to the DMD locusGenomics, 1990
- Åland Island eye disease (Forsius‐Eriksson ocular albinism) and an Xp21 deletion in a patient with duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasiaAmerican Journal of Medical Genetics, 1990
- Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markersCytogenetic and Genome Research, 1990
- A Common Language for Physical Mapping of the Human GenomeScience, 1989
- Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia.Journal of Clinical Investigation, 1989
- Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosomeAmerican Journal of Medical Genetics, 1988
- Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplificationNucleic Acids Research, 1988
- Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasiaHuman Genetics, 1987
- Infantile glycerol kinase deficiency— a condition requiring prompt identificationEuropean Journal of Pediatrics, 1987