Search Results - Wooderchak, W

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  1. 1
    Molecular diagnosis in hereditary hemorrhagic telangiectasia: findings in a series tested simultaneously by sequencing and deletion/duplication analysis

    Molecular diagnosis in hereditary hemorrhagic telangiectasia: findings in a series tested simultaneously by sequencing and deletion/duplication analysis by McDonald, J, Damjanovich, K, Millson, A, Wooderchak, W, Chibuk, JM, Stevenson, DA, Gedge, F, Bayrak-Toydemir, P

    Published in Clinical genetics
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  2. 2
    Hereditary hemorrhagic telangiectasia: two distinct ENG deletions in one family

    Hereditary hemorrhagic telangiectasia: two distinct ENG deletions in one family by Wooderchak, W, Gedge, F, McDonald, M, Krautscheid, P, Wang, X, Malkiewicz, J, Bukjiok, CJ, Lewis, T, Bayrak-Toydemir, P

    Published in Clinical genetics
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  3. 3
    An enzyme-coupled continuous spectrophotometric assay for S-adenosylmethionine-dependent methyltransferases

    An enzyme-coupled continuous spectrophotometric assay for S-adenosylmethionine-dependent methyltransferases by Dorgan, Kathleen M., Wooderchak, Whitney L., Wynn, DonRaphael P., Karschner, Erin L., Alfaro, Joshua F., Cui, Yinqiu, Zhou, Zhaohui Sunny, Hevel, Joan M.

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  4. 4
    BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia

    BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia by Wooderchak-Donahue, Whitney L., McDonald, Jamie, O’Fallon, Brendan, Upton, Paul D., Li, Wei, Roman, Beth L., Young, Sarah, Plant, Parker, Fülöp, Gyula T., Langa, Carmen, Morrell, Nicholas W., Botella, Luisa M., Bernabeu, Carmelo, Stevenson, David A., Runo, James R., Bayrak-Toydemir, Pinar

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  5. 5
    Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an “HHT‐like” syndrome in children

    Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an “HHT‐like” syndrome in children by Hodgson, Joshua, Ruiz‐Llorente, Lidia, McDonald, Jamie, Quarrell, Oliver, Ugonna, Kelechi, Bentham, James, Mason, Rebecca, Martin, Jennifer, Moore, David, Bergstrom, Katie, Bayrak‐Toydemir, Pinar, Wooderchak‐Donahue, Whitney, Morrell, Nicholas W., Condliffe, Robin, Bernabeu, Carmelo, Upton, Paul D.

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  6. 6
    Executive summary of the 11th HHT international scientific conference

    Executive summary of the 11th HHT international scientific conference by Arthur, Helen, Geisthoff, Urban, Gossage, James R., Hughes, Christopher C. W., Lacombe, Pascal, Meek, Mary E., Oh, Paul, Roman, Beth L., Trerotola, Scott O., Velthuis, Sebastiaan, Wooderchak-Donahue, Whitney

    Published in Angiogenesis (London)
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