Rajaa Fathallah

3PUBLICATIONS
11CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)
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Publications (3)

|Mar 20, 2026
IVNS1ABP mutation drives cellular senescence in newly identified progeroid neuropathy.

Fang Yuan, Ye Sing Tan, Haofei Wang

|Aug 03, 2025
Outcomes of genetic testing and prenatal diagnosis of spinal muscular atrophy in Jordan.

Mohammad Shboul, Mohammed El-Khateeb, Rajaa Fathallah

|Jul 28, 2025
Whole-exome sequencing for prenatal diagnosis of fetal anomalies: insights from a Jordanian cohort.

Mohammad Shboul, Nadia Badaro, Reem Darweesh

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