Herdanza non mendeliana (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "Herdanza non mendeliana" in Galician language version.

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annualreviews.org

Santoro, MR; Bray SM, Warren ST. (2012). "Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective". Annu. Rev. Pathol. Mech. Dis. 7: 219–45. doi:10.1146/annurev-pathol-011811-132457. PMID 22017584. http://www.annualreviews.org/doi/abs/10.1146/annurev-pathol-011811-132457 Arquivado 23 de maio de 2016 en Wayback Machine..

Klug, William S.; Michael R. Cummings, Charlotte A. Spencer (2006). Concepts of Genetics. Upper Saddle River, NJ: Pearson Education Inc. p. 215.

Van Heyningen V, Yeyati PL (2004). "Mechanisms of non-Mendelian inheritance in genetic disease". Hum. Mol. Genet. 13 Spec No 2: R225–33. PMID 15358729. doi:10.1093/hmg/ddh254.
Mitchell MB, Mitchell HK (1952). "A case of "maternal" inheritance in Neurospora crassa". Proc. Natl. Acad. Sci. U.S.A. 38 (5): 442–9. PMC 1063583. PMID 16589122. doi:10.1073/pnas.38.5.442.
Embley, T. Martin; William Martin (2006). "Eukaryotic evolution, changes and challenges". Nature 440 (7084): 623–630. PMID 16572163. doi:10.1038/nature04546.
Bell, A.C.; G. Felsenfeld (2000). "Methylation of a CTCF-dependent boundar control imprinted expression of the Igf2 gene". Nature 405 (6785): 482–485. PMID 10839546. doi:10.1038/35013100.
Chen J, Cooper DN, Chuzhanova N, Férec C, Patrinos GP. (2007). "Gene conversion: mechanisms, evolution and human disease". Nature Reviews Genetics 8: 762–775. PMC 2779867. PMID 17846636. doi:10.1038/nrg2193.

Van Heyningen V, Yeyati PL (2004). "Mechanisms of non-Mendelian inheritance in genetic disease". Hum. Mol. Genet. 13 Spec No 2: R225–33. PMID 15358729. doi:10.1093/hmg/ddh254.
Mitchell MB, Mitchell HK (1952). "A case of "maternal" inheritance in Neurospora crassa". Proc. Natl. Acad. Sci. U.S.A. 38 (5): 442–9. PMC 1063583. PMID 16589122. doi:10.1073/pnas.38.5.442.
Embley, T. Martin; William Martin (2006). "Eukaryotic evolution, changes and challenges". Nature 440 (7084): 623–630. PMID 16572163. doi:10.1038/nature04546.
Bell, A.C.; G. Felsenfeld (2000). "Methylation of a CTCF-dependent boundar control imprinted expression of the Igf2 gene". Nature 405 (6785): 482–485. PMID 10839546. doi:10.1038/35013100.
Chen J, Cooper DN, Chuzhanova N, Férec C, Patrinos GP. (2007). "Gene conversion: mechanisms, evolution and human disease". Nature Reviews Genetics 8: 762–775. PMC 2779867. PMID 17846636. doi:10.1038/nrg2193.
Santoro, MR; Bray SM, Warren ST. (2012). "Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective". Annu. Rev. Pathol. Mech. Dis. 7: 219–45. doi:10.1146/annurev-pathol-011811-132457. PMID 22017584. http://www.annualreviews.org/doi/abs/10.1146/annurev-pathol-011811-132457 Arquivado 23 de maio de 2016 en Wayback Machine..

Santoro, MR; Bray SM, Warren ST. (2012). "Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective". Annu. Rev. Pathol. Mech. Dis. 7: 219–45. doi:10.1146/annurev-pathol-011811-132457. PMID 22017584. http://www.annualreviews.org/doi/abs/10.1146/annurev-pathol-011811-132457 Arquivado 23 de maio de 2016 en Wayback Machine..