Azzeddine Laaraje

3PUBLICATIONS
4CO-AUTHORS
Developmental genetics (incl. sex determination)Medical biotechnology diagnostics (incl. biosensors)Aboriginal and Torres Strait Islander artefacts
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Publications (3)

|Mar 11, 2026
Novel ANKRD11 Mutation in KBG Syndrome: A diagnostic triad of hearing loss, radiological macrodontia and artificial intelligence-assisted facial phenotyping.

Azzeddine Laaraje, Khadija Belcadi Abassi, Mouna Lemaamer

|Sep 22, 2025
Novel MCT8 mutation: diagnostic value of T3/T4 ratio.

Azzeddine Laaraje, Abdelilah Radi, Soukaina Ait Hmadouch

|Sep 22, 2025
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay with Early-Onset Epilepsy and Novel Clinical Features: A rare entity from Morocco in the Middle East and North Africa region.

Azzeddine Laaraje, Basma Alaoui, Abdelilah Radi

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Frequent Collaborators

2 joint publications

Abdelilah Radi

2 joint publications

Rachid Abilkassem

1 joint publications

Khadija Belcadi Abassi

1 joint publications

Mouna Lemaamer