NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan population von El Bouchikhi, Ihssane, Bouguenouch, Laila, Zohra Moufid, Fatima, Houssaini, Mohammed Iraqui, Belhassan, Khadija, Samri, Imane, Joutei, Ayoub Tahri, Ouldim, Karim, Atmani, Samir

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

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GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot von EL Bouchikhi, Ihssane, Belhassan, Khadija, Moufid, Fatima Zohra, Houssaini, Mohammed Iraqui, Bouguenouch, Laila, Samri, Imane, Bouhrim, Mohamed, Ouldim, Karim, Atmani, Samir

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

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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 von El Bouchikhi, Ihssane, Bouguenouch, Laila, Moufid, Fatima Zohra, Belhassan, Khadija, Samri, Imane, Chaouti, Amal, Houssaïni, Mohammed Iraqui, Atmani, Samir, Ouldim, Karim

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

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Novel NKX2-5 germline mutation in a Moroccan child with transitional atrio-ventricular septal defect (tAVSD) von El-Bouchikhi, Ihssane, Belhassan, Khadija, Moufid, Fatima Zohra, Houssaini, Mohammed Iraqui, Ouldim, Karim, Atmani, Samir

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Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rate von El Bouchikhi, Ihssane, Belhassan, Khadija, Moufid, Fatima Zohra, Iraqui Houssaini, Mohammed, Bouguenouch, Laila, Samri, Imane, Atmani, Samir, Ouldim, Karim

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