Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: Evidence of non-linkage
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference9 articles.
1. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
2. (1992) “Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive and X-Linked Phenotypes,” 10th ed. Baltimore: The Johns Hopkins University Press.
3. Rapid transfer of DNA from agarose gels to nylon membranes
4. Pathophysiology of neurofibromatosis
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