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Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1.
A two year experience of DNA diagnosis for NF1 is presented. Twenty-three NF1 families have been analysed using 11 closely linked and intragenic markers. Prenatal testing was undertaken for six families; 11 affected subjects and their partners wished to know if they would be informative for future p...
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| Udgivet i: | J Med Genet |
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| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BMJ Publishing Group
1992
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015893/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1348093/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.29.3.180 |
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