Nome's disease: close linkage with genetic markers from the proximal short arm of the X chromosome
- 1 March 1985
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 27 (3), 282-283
- https://doi.org/10.1111/j.1399-0004.1985.tb00221.x
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28Nature, 1984
- Report of the committee on human gene mapping by recombinant DNA techniquesCytogenetic and Genome Research, 1984
- C‐heteromorphism in the human X‐chromosome SirsClinical Genetics, 1982
- DNA sequence variants in the Gγ-, Aγ-, δ- and β-globin genes of manCell, 1979