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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2006 | 1 |
2008 | 2 |
2024 | 0 |
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Expanding the clinical spectrum of MYCN-related Feingold syndrome.
Am J Med Genet A. 2006 Oct 15;140(20):2254-6. doi: 10.1002/ajmg.a.31407.
Am J Med Genet A. 2006.
PMID: 16906565
No abstract available.
Genotype-phenotype correlations in MYCN-related Feingold syndrome.
Marcelis CL, Hol FA, Graham GE, Rieu PN, Kellermayer R, Meijer RP, Lugtenberg D, Scheffer H, van Bokhoven H, Brunner HG, de Brouwer AP.
Marcelis CL, et al.
Hum Mutat. 2008 Sep;29(9):1125-32. doi: 10.1002/humu.20750.
Hum Mutat. 2008.
PMID: 18470948
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Feingold syndrome associated with two novel MYCN mutations in sporadic and familial cases including monozygotic twins.
Blaumeiser B, Oehl-Jaschkowitz B, Borozdin W, Kohlhase J.
Blaumeiser B, et al.
Am J Med Genet A. 2008 Sep 1;146A(17):2304-7. doi: 10.1002/ajmg.a.32444.
Am J Med Genet A. 2008.
PMID: 18671284
No abstract available.
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