Hasil Pencarian - Katarzyna Falana

  • Menampilkan 1 - 3 hasil dari 3
Perbaiki Hasil
  1. 1
    Identification of a novel inherited ALK variant M1199L in the WNT type of medulloblastoma

    Identification of a novel inherited ALK variant M1199L in the WNT type of medulloblastoma oleh Joanna Trubicka, Małgorzata Szperl, Wiesława Grajkowska, Agnieszka Karkucińska-Więckowska, Magdalena Tarasińska, Katarzyna Falana, Bożenna Dembowska-Bagińska, Maria Łastowska

    Diterbitkan 2016-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    Malan syndrome (Sotos syndrome 2) in two patients with 19p13.2 deletion encompassing NFIX gene and novel NFIX sequence variant

    Malan syndrome (Sotos syndrome 2) in two patients with 19p13.2 deletion encompassing NFIX gene and novel NFIX sequence variant oleh Aleksandra Jezela-Stanek, Marzena Kucharczyk, Katarzyna Falana, Dorota Jurkiewicz, Marlena Mlynek, Dorota Wicher, Malgorzata Rydzanicz, Monika Kugaudo, Agata Cieslikowska, Elzbieta Ciara, Rafal Ploski, Malgorzata Krajewska-Walasek

    Diterbitkan 2016-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    The germline variants in DNA repair genes in pediatric medulloblastoma: a challenge for current therapeutic strategies

    The germline variants in DNA repair genes in pediatric medulloblastoma: a challenge for current therapeutic strategies oleh Joanna Trubicka, Tomasz Żemojtel, Jochen Hecht, Katarzyna Falana, Dorota Piekutowska- Abramczuk, Rafał Płoski, Marta Perek-Polnik, Monika Drogosiewicz, Wiesława Grajkowska, Elżbieta Ciara, Elżbieta Moszczyńska, Bożenna Dembowska-Bagińska, Danuta Perek, Krystyna H. Chrzanowska, Małgorzata Krajewska-Walasek, Maria Łastowska

    Diterbitkan 2017-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: