Showing 121 - 140 results of 1,106 for search '"Boys ', query time: 0.06s Refine Results
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    The Adventures of Huckleberry Finn / by Twain, Mark

    Published 1876
    Subjects:
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    Book
  3. 123

    A Case of a 5-Year-Old Boy with a Blauth Type IIIB Hypoplastic Thumb Reconstructed with a Nonvascularized, Hemilongitudinal Metatarsal Transfer by Mika Nakada, Kaoru Tada, Tadahiro Nakajima, Masashi Matsuta, Hiroyuki Tsuchiya

    Published 2018-01-01
    “…We performed a nonvascularized, hemilongitudinal metatarsal bone transfer on a 5-year-old boy with a type IIIB hypoplastic thumb. Despite the child’s age, the growth of the thumb was confirmed and the thumb had stabilized. …”
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  4. 124

    The Partial Duplication of the 5′ Segment of KMT2A Revealed KMT2A-MLLT10 Rearrangement in a Boy with Acute Myeloid Leukemia by Hiroko Fukushima, Toru Nanmoku, Sho Hosaka, Yuni Yamaki, Nobutaka Kiyokawa, Takashi Fukushima, Ryo Sumazaki

    Published 2017-01-01
    “…The duplication of 5′ segment of KMT2A is a rare molecular event in childhood leukemia, and the influence on prognosis is unknown. Here, we report on a boy who developed acute monocytic leukemia. Fluorescence in situ hybridization revealed the duplication of the 5′ segment with 2 normal alleles at KMT2A which was eventually found to be fused with MLLT10. …”
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    PENGUJIAN TIGA VARIETAS JAGUNG MANIS (Zea mays saccharata) DI RUMBAI KOTA PEKANBARU by Surtinah Surtinah

    Published 2015-08-01
    Subjects: “…Key Words : Jagung Manis, Super Sweet, Bonanza, Sweet Boy…”
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    Implementing Shoah-Themed Literature into Teaching with the Example of <i>The Boy From Block 66: A WW2 Jewish Holocaust Survival True Story</i> by Milan Mašát

    Published 2025-01-01
    Subjects: “…<i>The Boy From Block 66: A WW2 Jewish Holocaust Survival True Story</i>…”
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    X-Linked Adrenal Hypoplasia Congenita in a Boy due to a Novel Deletion of the Entire NR0B1 (DAX1) and MAGEB1–4 Genes by Aleksandra Rojek, Maciej R. Krawczynski, Aleksander Jamsheer, Anna Sowinska-Seidler, Barbara Iwaniszewska, Ewa Malunowicz, Marek Niedziela

    Published 2016-01-01
    “…X-linked Adrenal Hypoplasia Congenita (AHC) is caused by deletions or point mutations in the NR0B1 (DAX1) gene. We present a boy with AHC who came at the age of 25 days in a severe state due to prolonged vomiting and progressive dehydration. …”
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