Works matching AU SHEN Wei


Results: 2262
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    Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene.

    Published in:
    Human Mutation, 2018, v. 39, n. 11, p. 1569, doi. 10.1002/humu.23649
    By:
    • Zastrow, Diane B.;
    • Baudet, Heather;
    • Shen, Wei;
    • Thomas, Amanda;
    • Si, Yue;
    • Weaver, Meredith A.;
    • Lager, Angela M.;
    • Liu, Jixia;
    • Mangels, Rachel;
    • Dwight, Selina S.;
    • Wright, Matt W.;
    • Dobrowolski, Steven F.;
    • Eilbeck, Karen;
    • Enns, Gregory M.;
    • Feigenbaum, Annette;
    • Lichter‐Konecki, Uta;
    • Lyon, Elaine;
    • Pasquali, Marzia;
    • Watson, Michael;
    • Blau, Nenad
    Publication type:
    Article
    47

    Cover Image, Volume 39, Issue 11.

    Published in:
    Human Mutation, 2018, v. 39, n. 11, p. i, doi. 10.1002/humu.23662
    By:
    • Zastrow, Diane B.;
    • Baudet, Heather;
    • Shen, Wei;
    • Thomas, Amanda;
    • Si, Yue;
    • Weaver, Meredith A.;
    • Lager, Angela M.;
    • Liu, Jixia;
    • Mangels, Rachel;
    • Dwight, Selina S.;
    • Wright, Matt W.;
    • Dobrowolski, Steven F.;
    • Eilbeck, Karen;
    • Enns, Gregory M.;
    • Feigenbaum, Annette;
    • Lichter‐Konecki, Uta;
    • Lyon, Elaine;
    • Pasquali, Marzia;
    • Watson, Michael;
    • Blau, Nenad
    Publication type:
    Article
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