Publications by authors named "Ihssane El Bouchikhi"

11Publications

Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation.

Turk J Gastroenterol 2018 11;29(6):701-704

Department of Medical Genetics and Oncogenetics, Centre Hospitalier Universitaire Hassan II, Fez, Morocco; Laboratory of Biomedical and Translational Research, Faculté de Médecine et de Pharmacie de Fès (FMPF), Université Sidi Mohammed Ben Abdellah (USMBA), Fez, Morocco.

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November 2018

Novel NKX2-5 germline mutation in a Moroccan child with transitional atrio-ventricular septal defect (tAVSD).

Turk J Pediatr 2017 ;59(5):610-613

Medico-Surgical Unit of Cardio-pediatrics, Department of Pediatrics, Hassan II University Hospital, Fez, Morocco.

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January 2019

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

Int J Pediatr Adolesc Med 2016 Dec 18;3(4):133-142. Epub 2016 Aug 18.

Medical Genetics and Oncogenetics Laboratory, HASSAN II University Hospital, BP 1835, Atlas, Fez 30000, Morocco.

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December 2016