APA
Makrythanasis P., Nelis M., Santoni F. A., Guipponi M., Vannier A., Béna F., Gimelli S., Stathaki E., Temtamy S., Mégarbané A., Masri A., Aglan M. S., Zaki M. S., Bottani A., Fokstuen S., Gwanmesia L., Aliferis K., Bustamante Eduardo M., Stamoulis G., Psoni S., Kitsiou-Tzeli S., Fryssira H., Kanavakis E., Al-Allawi N., Sefiani A., Al Hait S., Elalaoui S. C., Jalkh N., Al-Gazali L., Al-Jasmi F., Bouhamed H. C., Abdalla E., Cooper D. N., Hamamy H. & Antonarakis S. E. (20150609). Diagnostic exome sequencing to elucidate the genetic basis of likely recessive disorders in consanguineous families. : Human mutation.
Chicago
Makrythanasis Periklis, Nelis Mari, Santoni Federico A, Guipponi Michel, Vannier Anne, Béna Frédérique, Gimelli Stefania, Stathaki Elisavet, Temtamy Samia, Mégarbané André, Masri Amira, Aglan Mona S, Zaki Maha S, Bottani Armand, Fokstuen Siv, Gwanmesia Lorraine, Aliferis Konstantinos, Bustamante Eduardo Mariana, Stamoulis Georgios, Psoni Stavroula, Kitsiou-Tzeli Sofia, Fryssira Helen, Kanavakis Emmanouil, Al-Allawi Nasir, Sefiani Abdelaziz, Al Hait Sana', Elalaoui Siham C, Jalkh Nadine, Al-Gazali Lihadh, Al-Jasmi Fatma, Bouhamed Habiba Chaabouni, Abdalla Ebtesam, Cooper David N, Hamamy Hanan and Antonarakis Stylianos E. 20150609. Diagnostic exome sequencing to elucidate the genetic basis of likely recessive disorders in consanguineous families. : Human mutation.
Harvard
Makrythanasis P., Nelis M., Santoni F. A., Guipponi M., Vannier A., Béna F., Gimelli S., Stathaki E., Temtamy S., Mégarbané A., Masri A., Aglan M. S., Zaki M. S., Bottani A., Fokstuen S., Gwanmesia L., Aliferis K., Bustamante Eduardo M., Stamoulis G., Psoni S., Kitsiou-Tzeli S., Fryssira H., Kanavakis E., Al-Allawi N., Sefiani A., Al Hait S., Elalaoui S. C., Jalkh N., Al-Gazali L., Al-Jasmi F., Bouhamed H. C., Abdalla E., Cooper D. N., Hamamy H. and Antonarakis S. E. (20150609). Diagnostic exome sequencing to elucidate the genetic basis of likely recessive disorders in consanguineous families. : Human mutation.
MLA
Makrythanasis Periklis, Nelis Mari, Santoni Federico A, Guipponi Michel, Vannier Anne, Béna Frédérique, Gimelli Stefania, Stathaki Elisavet, Temtamy Samia, Mégarbané André, Masri Amira, Aglan Mona S, Zaki Maha S, Bottani Armand, Fokstuen Siv, Gwanmesia Lorraine, Aliferis Konstantinos, Bustamante Eduardo Mariana, Stamoulis Georgios, Psoni Stavroula, Kitsiou-Tzeli Sofia, Fryssira Helen, Kanavakis Emmanouil, Al-Allawi Nasir, Sefiani Abdelaziz, Al Hait Sana', Elalaoui Siham C, Jalkh Nadine, Al-Gazali Lihadh, Al-Jasmi Fatma, Bouhamed Habiba Chaabouni, Abdalla Ebtesam, Cooper David N, Hamamy Hanan and Antonarakis Stylianos E. Diagnostic exome sequencing to elucidate the genetic basis of likely recessive disorders in consanguineous families. : Human mutation. 20150609.