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Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.
Eleven families with Noonan syndrome in either two or three generations have been identified. Following the reports of subjects with features of both Noonan syndrome and neurofibromatosis type 1, these pedigrees have been studied using a number of probes at the neurofibromatosis type 1 locus (17q11)...
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| Veröffentlicht in: | J Med Genet |
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| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMJ Publishing Group
1992
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015895/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1348095/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.29.3.188 |
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