Publications by authors named "Moustafa Hamchou"

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A novel missense heterozygous mutation in MAP3K1 gene causes 46, XY disorder of sex development: case report and literature review.
Aisha Al Shamsi, Noura Al Hassani, Moustafa Hamchou, Raya Almazrouei, Aziz Mhanni

Mol Genet Genomic Med· November 2020

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Segmental omental infarction: a rare cause of acute abdominal pain in children.
Moustafa Hamchou, Mukul Kothari, Bahjat Sahari, Adnan Swid, Ahmed H Al-Salem

Surg Laparosc Endosc Percutan Tech· February 2014

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Colonic adenocarcinoma as a secondary malignancy after treatment of embryonal rhabdomyosarcoma.
Moustafa Hamchou, Hilal Matta, Gabriel Ionescu, Adnan Swid, Ahmed H Al-Salem

World J Pediatr· February 2013

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Familial achalasia in children.
Fawaz Chikh Torab, Moustafa Hamchou, Gabriel Ionescu, Ahmed H Al-Salem

Pediatr Surg Int· December 2012

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