Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8.

Author:

Diehl S R,Boehnke M,Collins F S,Erickson R P,Karolyi I J,Ploughman L M,Pericak-Vance M A,Aylsworth A S,Roses A D

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference10 articles.

1. Juvenile chronic granulocytic leukemia in a patient with trisomy 8, neurofibromatosis, and prolonged Epstein-Barr virus infection;Palmer, C.G.; Provisor, A.J.; Weaver, D.D.;J Pediatr,1983

2. Linkage studies in peripheral neurofibromatosis;Pericak-Vance, M.A.; Yamaoka, L.H.; Vance, J.M.;J Med Genet,1987

3. Basic methods in molecular biology;Davis, L.G.; Dibner, M.D.; Battey, J.F.,1986

4. The human thyroglobulin gene: a polymorphic marker localised distal to cmyc;Baas, F.; Bikker, H.; Geurts van Kessel, A.

5. Human tissue-type plasminogen activator gene located near chromosomal breakpoint in myeloproliferative disorder;Yang-Feng, T.L.; Opdenakker, G.; Volckaert, G.; Francke, U.;Am J Hum Genet,1986

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