Allele-Specific Non-CpG Methylation of the Nf1 Gene during Early Mouse Development von Haines, Thomas R., Rodenhiser, David I., Ainsworth, Peter J.

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CpG methylation within the 5' regulatory region of the BRCA1 gene is tumor specific and includes a putative CREB binding site von MANCINI, D. N, RODENHISER, D. I, AINSWORTH, P. J, O'MALLEY, F. P, SINGH, S. M, WEIRONG XING, ARCHER, T. K

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Pathological findings in the x-linked form of Charcot-Marie-Tooth disease : a morphometric and ultrastructural analysis von HAHN, Angelika F, AINSWORTH, Peter J, BOLTON, Charles F, BILBAO, Juan M, VALLAT, Jean-Michel

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Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG→ATG) mutation von Feldman, Gerald L., Edmonds, Merrill W., Ainsworth, Peter J., Schuffenecker, Isabelle, Lenoir, Gilbert M., Saxe, Andrew W., Talpos, Gary B., Roberson, Jacquelyn, Petrucelli, Nancie, Jackson, Charles E.

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Genotype/Phenotype Correlations in X-Linked Dominant Charcot-Marie-Tooth Disease von Hahn, Angelika F, Bolton, Charles F, White, Christopher M, Brown, William F, Tuuha, Sascha E, Tan, Charles C, Ainsworth, Peter J

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A model for GFR alpha 4 function and a potential modifying role in multiple endocrine neoplasia 2 von Vanhorne, Judith B, Andrew, Scott D, Harrison, Karen J, Taylor, Sherryl A M, Thomas, Bradley, McDonald, Thomas J, Ainsworth, Peter J, Mulligan, Lois M

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Clinical and pathological observations in men lacking the gap junction protein connexin 32 von Hahn, Angelika F., Ainsworth, Peter J., Naus, Christian C. G., Mao, Jian, Bolton, Charles F.

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Family cancer histories predictive of a high risk of hereditary non-polyposis colorectal cancer associate significantly with a genomic rearrangement in hMSH2 or hMLH1 von Ainsworth, PJ, Koscinski, D., Fraser, BP, Stuart, JA

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Example of somatic mosaicism in a series of de novo neurofibromatosis type 1 cases due to a maternally derived deletion von Ainsworth, PJ, Chakraborty, PK, Weksberg, R

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Genotype/phenotype correlation in affected individuals of a family with a deletion of the entire coding sequence of the connexin 32 gene von AINSWORTH, P. J, BOLTON, C. F, MURPHY, B. C, STUART, J. A, HAHN, A. F

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Individual and family characteristics associated with protein truncating BRCA1 and BRCA2 mutations in an Ontario population based series from the Cooperative Family Registry for Br... von Ozcelik, H, Knight, J A, Glendon, G, Yazici, H, Carson, N, Ainsworth, P J, Taylor, S A M, Feilotter, H, Carter, R F, Boyd, N F, Andrulis, I L

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Novel mutations in the connexin 32 gene associated with X-linked Charcot-Marie tooth disease von Tan, Charles C., Ainsworth, Peter J., Hahn, Angelika F., MacLeod, Patrick M.

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Identification and characterization of sporadic and inherited mutations in exon 31 of the neurofibromatosis (NF1) gene von AINSWORTH, P. J, RODENHISER, D. I, COSTA, M. T

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Intramolecular diels-alder reactions of silyl acetal-tethered trienes von J. Ainsworth, Peter, Craig, Donald, C. Reader, John, M.Z. Slawin, Alexandra, J.P. White, Andrew, J. Williams, David

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Intramolecular Diels-Alder reactions of carbon acetal-tethered trienes von Ainsworth, Peter J., Craig, Donald, White, Andrew J.P., Williams, David J.

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A double mutation in exon 6 of the β-hexosaminidase α subunit in a patient with the B1 variant of Tay-Sachs disease von AINSWORTH, P. J, COULTER-MACKIE, M. B

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Intramolecular Diels-Alder reactions of trienes tethered with an ether linkage von Ainsworth, Peter J., Craig, Donald, Reader, John C., Slawin, Alexandra M.Z., White, Andrew J.P., Williams, David J.

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A five-basepair deletion (7118 delTTTTA) identified within neurofibromatosis (NF1) exon 39 von Rodenhiser, D I, Jung, J H, Gillett, J M, Hovland, K, Andrews, J, Ainsworth, P J, Coulter-Mackie, M, Singh, S M

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A nongenetic basis of cycle frequency in bipolar disorder : Study of a monozygotic twin pair von SHARMA, V, AINSWORTH, P. J, MCCABE, S. B, PERSAD, E, KUENEMAN, K. M

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Membrane phase transitions as a diagnostic tool for studying mitochondriogenesis von Ainsworth, P.J., Tustanoff, E.Reno, Ball, A.J.S.

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