Publications by authors named "Layla Zniber"

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Post-mortem diagnosis of Pompe disease by exome sequencing in a Moroccan family: a case report.
Najlae Adadi, Maryem Sahli, Grégory Egéa, Ilham Ratbi, Mohamed Taoudi, Layla Zniber

J Med Case Rep· October 2018

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Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death.
Najim Lahrouchi, Elisabeth M Lodder, Maria Mansouri, Rafik Tadros, Layla Zniber

Eur J Hum Genet· June 2017

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The Boy from Fez: A tale of five charities, and the global community, joining hands.
Layla Zniber, Maria Rogers, Akhlaque Nabi Bhat, Ahmad Sallehuddin, Lisa Yacoub

Glob Cardiol Sci Pract· April 2014

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Congenital rubella syndrome burden in Morocco: a rapid retrospective assessment.
Sharon Bloom, Ahmed Rguig, Amina Berraho, Layla Zniber, Naima Bouazzaoui

Lancet· February 2005

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