Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger-Huët anomaly (Q28587547)

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Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger-Huët anomaly
scientific journal article

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    title
    Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger-Huët anomaly (English)
    1 reference
    stated in
    PubMed
    PubMed ID
    20577004
    retrieved
    31 January 2017
    author
    Nadezda Maksimova
    object named as
    Nadezda Maksimova
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    1
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    Osamu Onodera
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    Osamu Onodera
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    17
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    author name string
    Kenju Hara
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    2
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    PubMed
    PubMed ID
    20577004
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    31 January 2017
    Irina Nikolaeva
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    3
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    PubMed
    PubMed ID
    20577004
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    31 January 2017
    Tan Chun-Feng
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    4
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    PubMed
    PubMed ID
    20577004
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    31 January 2017
    Tomoaki Usui
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    5
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    PubMed
    PubMed ID
    20577004
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    Mineo Takagi
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    6
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    20577004
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    31 January 2017
    Yasushi Nishihira
    series ordinal
    7
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    PubMed ID
    20577004
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    31 January 2017
    Akinori Miyashita
    series ordinal
    8
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    PubMed ID
    20577004
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    Hiroshi Fujiwara
    series ordinal
    9
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    PubMed ID
    20577004
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    Tokuhide Oyama
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    10
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    PubMed ID
    20577004
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    Anna Nogovicina
    series ordinal
    11
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    PubMed ID
    20577004
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    31 January 2017
    Aitalina Sukhomyasova
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    12
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    PubMed
    PubMed ID
    20577004
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    Svetlana Potapova
    series ordinal
    13
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    PubMed ID
    20577004
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    Ryozo Kuwano
    series ordinal
    14
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    PubMed
    PubMed ID
    20577004
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    Hitoshi Takahashi
    series ordinal
    15
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    PubMed ID
    20577004
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    31 January 2017
    Masatoyo Nishizawa
    series ordinal
    16
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    stated in
    PubMed
    PubMed ID
    20577004
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    31 January 2017
    publication date
    1 August 2010
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    PubMed
    PubMed ID
    20577004
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    31 January 2017
    volume
    47
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    20577004
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    issue
    8
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    PubMed
    PubMed ID
    20577004
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    31 January 2017
    page(s)
    538–548
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    PubMed
    PubMed ID
    20577004
    retrieved
    31 January 2017
    cites work

    Identifiers

    PMCID
    2921285
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