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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Detalles Bibliográficos
Autores principales: 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.
Formato: Artigo
Lenguaje:Inglês
Publicado: 1989
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Original Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715468/
https://ncbi.nlm.nih.gov/pubmed/2491778
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