Hasil Pencarian - Fatima Zohra Moufid

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  1. 1
    P048: Novel frameshift MLH1 germline mutation in a Moroccan Lynch syndrome family

    P048: Novel frameshift MLH1 germline mutation in a Moroccan Lynch syndrome family oleh Abdelhamid Bouramtane, Fatima Zohra Moufid, Mohamed Ahakoud, Laila Bouguenouch, Karim Ouldim

    Diterbitkan 2023-01-01
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  2. 2
    Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype

    Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype oleh Ihssane EL Bouchikhi, Khadija Belhassan, Fatima Zohra Moufid, Laila Bouguenouch, Imane Samri, Mohammed Iraqui Houssaïni, Karim Ouldim, Samir Atmani

    Diterbitkan 2021-03-01
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  3. 3
    Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects

    Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects oleh Ihssane El Bouchikhi, Laila Bouguenouch, Fatima Zohra Moufid, Khadija Belhassan, Imane Samri, Amal Chaouti, Mohammed Iraqui Houssaïni, Samir Atmani, Karim Ouldim

    Diterbitkan 2020-10-01
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  4. 4
    Molecular and environmental characterization of Noonan syndrome in Morocco reveals a significant association with consanguinity and advanced parental age

    Molecular and environmental characterization of Noonan syndrome in Morocco reveals a significant association with consanguinity and advanced parental age oleh Ihssane El Bouchikhi, Laila Bouguenouch, Fatima Zohra Moufid, Imane Samri, Fatima Abdouss, Moulay Abdelilah Melhouf, Mohammed Iraqui Houssaini, Khadija Belhassan, Samir Atmani, Karim Ouldim

    Diterbitkan 2020-02-01
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