Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rate

por El Bouchikhi, Ihssane, Belhassan, Khadija, Moufid, Fatima Zohra, Iraqui Houssaini, Mohammed, Bouguenouch, Laila, Samri, Imane, Atmani, Samir, Ouldim, Karim
Publicado 2016

The detection of a novel insertion mutation in exon 2 of the MEFV gene associated with familial mediterranean fever in a moroccan family

por Mejtoute, Touhami, Sayel, Hanane, El-Akhal, Jamila, Moufid, Fatima Z., Bouguenouch, Laila, El Bouchikhi, Ihssane, Hida, Mustapha, Couissi, Driss, Ouldim, Karim
Publicado 2017

GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot

por EL Bouchikhi, Ihssane, Belhassan, Khadija, Moufid, Fatima Zohra, Houssaini, Mohammed Iraqui, Bouguenouch, Laila, Samri, Imane, Bouhrim, Mohamed, Ouldim, Karim, Atmani, Samir
Publicado 2018

Molecular and clinical assessment of maturity-onset diabetes of the young revealed low mutational rate in Moroccan families

por Trhanint, Said, Bouguenouch, Laila, Abourazzak, Sana, El Ouahabi, Hanan, Latrech, Hanane, Benyakhlef, Salma, Bennani, Bahia, El Bouchikhi, Ihssane, Moufid, Fatima Zahra, Ouldim, Karim, El Ghadraoui, Lahsen, Maazouzi, Nadia
Publicado 2022

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

por Škorić-Milosavljević, Doris, Lahrouchi, Najim, Bosada, Fernanda M., Dombrowsky, Gregor, Williams, Simon G., Lesurf, Robert, Tjong, Fleur V. Y., Walsh, Roddy, El Bouchikhi, Ihssane, Breckpot, Jeroen, Audain, Enrique, Ilgun, Aho, Beekman, Leander, Ratbi, Ilham, Strong, Alanna, Muenke, Maximilian, Heide, Solveig, Muir, Alison M., Hababa, Mariam, Cross, Laura, Zhou, Dihong, Pastinen, Tomi, Zackai, Elaine, Atmani, Samir, Ouldim, Karim, Adadi, Najlae, Steindl, Katharina, Rauch, Anita, Brook, David, Wilsdon, Anna, Kuipers, Irene, Blom, Nico A., Mulder, Barbara J., Mefford, Heather C., Keren, Boris, Joset, Pascal, Kruszka, Paul, Thiffault, Isabelle, Sheppard, Sarah E., Roberts, Amy, Lodder, Elisabeth M., Keavney, Bernard D., Clur, Sally-Ann B., Mital, Seema, Hitz, Marc-Philip, Christoffels, Vincent M., Postma, Alex V., Bezzina, Connie R.
Publicado 2021

Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

por Škorić-Milosavljević, Doris, Lahrouchi, Najim, Bosada, Fernanda M., Dombrowsky, Gregor, Williams, Simon G., Lesurf, Robert, Tjong, Fleur V. Y., Walsh, Roddy, El Bouchikhi, Ihssane, Breckpot, Jeroen, Audain, Enrique, Ilgun, Aho, Beekman, Leander, Ratbi, Ilham, Strong, Alanna, Muenke, Maximilian, Heide, Solveig, Muir, Alison M., Hababa, Mariam, Cross, Laura, Zhou, Dihong, Pastinen, Tomi, Zackai, Elaine, Atmani, Samir, Ouldim, Karim, Adadi, Najlae, Steindl, Katharina, Rauch, Anita, Brook, David, Wilsdon, Anna, Kuipers, Irene, Blom, Nico A., Mulder, Barbara J., Mefford, Heather C., Keren, Boris, Joset, Pascal, Kruszka, Paul, Thiffault, Isabelle, Sheppard, Sarah E., Roberts, Amy, Lodder, Elisabeth M., Keavney, Bernard D., Clur, Sally-Ann B., Mital, Seema, Hitz, Marc-Philip, Christoffels, Vincent M., Postma, Alex V., Bezzina, Connie R.
Publicado 2021