Treffer 1 - 4 von 4 für Suche 'Iskandarani, Alaa I', Suchdauer: 0,56s Treffer weiter einschränken
  1. 1
    Neuroblastoma amplified sequence gene mutation: A rare cause of recurrent liver failure in children

    Neuroblastoma amplified sequence gene mutation: A rare cause of recurrent liver failure in children von Hasosah, Mohammed Y, Iskandarani, Alaa I, Shawli, Ayman I, Alsahafi, Ashraf F, Sukkar, Ghassan A, Qurashi, Mansour A


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  2. 2
    Neuroblastoma amplified sequence gene mutation: A rare cause of recurrent liver failure in children

    Neuroblastoma amplified sequence gene mutation: A rare cause of recurrent liver failure in children von Hasosah, Mohammed Y, Iskandarani, Alaa I, Shawli, Ayman I, Alsahafi, Ashraf F, Sukkar, Ghassan A, Qurashi, Mansour A


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  3. 3
    Prenatal‐onset INPPL1‐related skeletal dysplasia in two unrelated families: Diagnosis and prediction of lethality

    Prenatal‐onset INPPL1‐related skeletal dysplasia in two unrelated families: Diagnosis and prediction of lethality von Abumansour, Iman Sabri, Iskandarani, Radiah Mahmoud, Edrees, Alaa, Javed, Farrukh, Taher, Fadwah, Hakeem, Ghaidaa Farouk

    Veröffentlicht in Clinical case reports

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  4. 4
    Prenatal-onset INPPL1-related skeletal dysplasia in two unrelated families: Diagnosis and prediction of lethality

    Prenatal-onset INPPL1-related skeletal dysplasia in two unrelated families: Diagnosis and prediction of lethality von Abumansour, Iman Sabri, Iskandarani, Radiah Mahmoud, Edrees, Alaa, Javed, Farrukh, Taher, Fadwah, Hakeem, Ghaidaa Farouk

    Veröffentlicht in Clinical case reports

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