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S Chafai Elalaoui

Showing results (1-10 of 4) with videos related to

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European Journal of Medical Genetics|February 16, 2010
Autosomal dominant microtiaS Chafai Elalaoui, I Cherkaoui Jaouad, L Rifai, et al.
BMC Medical Genetics|May 5, 2017
A novel TRPS1 mutation in a Moroccan family with Tricho-rhino-phalangeal syndrome type III: case reportW Smaili, S Chafai Elalaoui, S Meier, et al.
Journal Francais D'Ophtalmologie|January 9, 2010
[First North African observation of Leber congenital amaurosis secondary to CEP290 gene mutation]N Aboussair, A Berahou, I Perrault, et al.
European Journal of Medical Genetics|May 23, 2020
Exome sequencing revealed a novel homozygous METTL23 gene mutation leading to familial mild intellectual disability with dysmorphic featuresW Smaili, S Chafai Elalaoui, A Zrhidri, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
European Journal of Medical Genetics|February 16, 2010
Autosomal dominant microtiaS Chafai Elalaoui, I Cherkaoui Jaouad, L Rifai, et al.
BMC Medical Genetics|May 5, 2017
A novel TRPS1 mutation in a Moroccan family with Tricho-rhino-phalangeal syndrome type III: case reportW Smaili, S Chafai Elalaoui, S Meier, et al.
Journal Francais D'Ophtalmologie|January 9, 2010
[First North African observation of Leber congenital amaurosis secondary to CEP290 gene mutation]N Aboussair, A Berahou, I Perrault, et al.
European Journal of Medical Genetics|May 23, 2020
Exome sequencing revealed a novel homozygous METTL23 gene mutation leading to familial mild intellectual disability with dysmorphic featuresW Smaili, S Chafai Elalaoui, A Zrhidri, et al.
Pageof 1