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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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Vydáno v:J Med Genet
Hlavní autoři: Sharland, M, Taylor, R, Patton, M A, Jeffery, S
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Publishing Group 1992
Témata:
On-line přístup: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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