Mohammad Shboul
5PUBLICATIONS
26CO-AUTHORS
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Publications (5)
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|Oct 04, 2025
Genetic diagnosis of Jordanian patients with glycogen storage diseases.Mohammad Shboul, Mohammed El-Khateeb, Rajaa Fathallah
|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
|Jan 18, 2023
A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI-NET sequencing.Nasrinsadat Nabavizadeh, Annkatrin Bressin, Mohammad Shboul
|Oct 13, 2022
INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex.Lauren G Mascibroda, Mohammad Shboul, Nathan D Elrod
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Frequent Collaborators
2 joint publications
Mohammed El-Khateeb
2 joint publications
Nathalie Escande-Beillard
2 joint publications
Rajaa Fathallah
2 joint publications
Bruno Reversade
1 joint publications
Khadeeja Al-Rashed
1 joint publications
Nathan D Elrod
1 joint publications
Kai-Lieh Huang
1 joint publications
Moirangthem Kiran Singh
1 joint publications
Poojitha Sitaram
1 joint publications
Baeth Al-Rawashdeh
