Nada Amllal

4PUBLICATIONS
9CO-AUTHORS
Neurology and neuromuscular diseasesBioassaysEpigenetics (incl. genome methylation and epigenomics)
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Publications (4)

|Nov 08, 2024
Highlighting the different facets of SMC1A truncating variants: Two patients with novel SMC1A pathogenic variants.

Nada Amllal, Jaber Lyahyai, Lamiae Afif

|Sep 19, 2024
Novel variant related to SATB2-associated syndrome.

Nada Benyahya, Nada Amllal, Siham Chafai Elalaoui

|Aug 03, 2024
A series of four patients with Sotos syndrome harboring novel NSD1 mutations: clinical and molecular description.

Nada Amllal, Maria Zerkaoui, Wafaa Jdioui

|Sep 04, 2023
Identification of Two Novel ANKRD11 Mutations: Highlighting Incomplete Penetrance in KBG Syndrome.

Nada Amllal, Siham Chafai Elalaoui, Maria Zerkaoui

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