H. Elorch

Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly

V. Lougaris, A. Plebani, S. Lyonnet, 2019, Nature Communications.

Severe early onset retinitis pigmentosa in a Moroccan patient with Heimler syndrome due to novel homozygous mutation of PEX1 gene.

W. Newman, J. Lyahyai, I. Jaouad, 2016, European journal of medical genetics.

Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report

J. Lyahyai, A. Sefiani, A. Berraho, 2020, BMC medical genomics.

In-vivo Corneal Temperature during Cross-linking Measured by an Infrared Thermometer

A. Berraho, H. Elorch, H. Arsalane, 2018 .

Bilateral persistent pupillary membrane in an adult patient: A case report.

A. Berraho, F. Ibrahimi, H. Elorch, 2018, Journal francais d'ophtalmologie.

Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly

V. Lougaris, A. Plebani, S. Lyonnet, 2019, Nature Communications.