Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)

The defective gene causing von Recklinghausen neurofibromatosis (NF1), one of the most common inherited disorders affecting the human nervous system, was recently mapped to chromosome 17. We have used additional DNA markers to further narrow and bracket the NF1 defect. A multipoint linkage analysis...

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Bibliographic Details
Main Authors:	Seizinger, B. R., Farmer, G. E., Haines, J. L., Ozelius, L. J., Anderson, K., Korf, B. R., Parry, D. M., Pericak-Vance, M. A., Mulvihill, J. J., Menon, A., Hobbs, W. J., Martuza, R. L., Gusella, J. F.
Format:	Artigo
Language:	Inglês
Published:	1989
Subjects:	Original Articles
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC1715468/ https://ncbi.nlm.nih.gov/pubmed/2491778
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Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)

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