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Results:
1-7
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Results: 7
Authors:
Kelly, M
Edgar, AJ
Wevrick, R
Citation: M. Kelly et al., Analysis of DEXI/Dexi refines the organization of the mouse 7C and human 15q11 -> q13 imprinting clusters, CYTOG C GEN, 92(1-2), 2001, pp. 149-152
Authors:
Hanel, ML
Wevrick, R
Citation: Ml. Hanel et R. Wevrick, Establishment and maintenance of DNA methylation patterns in mouse Ndn: Implications for maintenance of imprinting in target genes of the imprinting center, MOL CELL B, 21(7), 2001, pp. 2384-2392
Authors:
Hanel, ML
Wevrick, R
Citation: Ml. Hanel et R. Wevrick, The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome, CLIN GENET, 59(3), 2001, pp. 156-164
Authors:
Lee, S
Kozlov, S
Hernandez, L
Chamberlain, SJ
Brannan, CI
Stewart, CL
Wevrick, R
Citation: S. Lee et al., Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype, HUM MOL GEN, 9(12), 2000, pp. 1813-1819
Authors:
Gilchrist, D
Glerum, DM
Wevrick, R
Citation: D. Gilchrist et al., Deconstructing Mendel: new paradigms in genetic mechanisms, CLIN INV M, 23(3), 2000, pp. 188-198
Authors:
Lee, S
Wevrick, R
Citation: S. Lee et R. Wevrick, Identification of novel imprinted transcripts in the Prader-Willi syndromeand Angelman syndrome deletion region: Further evidence for regional imprinting control, AM J HU GEN, 66(3), 2000, pp. 848-858
Authors:
Gerard, M
Hernandez, L
Wevrick, R
Stewart, CL
Citation: M. Gerard et al., Disruption of the mouse necdin gene results in early post-natal lethality, NAT GENET, 23(2), 1999, pp. 199-202
Risultati:
1-7
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