Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines

The fragile X syndrome is a very common disorder, but there has been little progress toward isolating the fragile X mutation (FRAXA). We describe a panel of 14 somatic cell hybrid lines, lymphoblastoid cell lines, and peripheral lymphocytes with X-chromosome translocation or deletion breakpoints nea...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Suthers, G. K., Hyland, V. J., Callen, D. F., Oberle, I., Rocchi, M., Thomas, N. S., Morris, C. P., Schwartz, C. E., Schmidt, M., Ropers, H. H., Baker, E., Oostra, B. A., Dahl, N., Wilson, P. J., Hopwood, J. J., Sutherland, G. R.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1990
Gaiak:
Original Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683725/
https://ncbi.nlm.nih.gov/pubmed/2378346
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