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Journal of Cosmetic Dermatology|February 1, 2021
Bioenergetic analysis of aged-phenotype skin in a rare syndromic cutis laxaNasrinsadat Nabavizadeh, Mohammad Shboul, Zohreh Hojati
The Application of Clinical Genetics|October 2, 2024
The Ser434Phe Androgen Receptor Gene Mutation Does Not Affect Fertility but is Associated with Increased ProlactinNesreen A Saadeh, Marya Obeidat, Mohammad Shboul
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|August 3, 2025
Outcomes of genetic testing and prenatal diagnosis of spinal muscular atrophy in JordanMohammad Shboul, Mohammed El-Khateeb, Rajaa Fathallah, et al.
The Turkish Journal of Pediatrics|September 28, 2019
Recessive mutation in GALNT3 causes hyperphosphatemic familial tumoral calcinosis associated with chronic recurrent multifocal osteomyelitisJumana Albaramki, Haitham Dmour, Mohammad Shboul, et al.
Current Biology : CB|January 19, 2016
Gmnc Is a Master Regulator of the Multiciliated Cell Differentiation ProgramFeng Zhou, Vijay Narasimhan, Mohammad Shboul, et al.
Biomedical Reports|August 2, 2024
Association between vitamin D metabolism gene polymorphisms and schizophreniaMohammad Shboul, Reem Darweesh, Abdulmalek Abu Zahraa, et al.
Non-Coding RNA Research|March 21, 2024
Plasma miRNAs as potential biomarkers for schizophrenia in a Jordanian cohortMohammad Shboul, Amal Bani Domi, Abdulmalek Abu Zahra, et al.
Journal of Investigative Medicine High Impact Case Reports|March 17, 2020
Tomographic Study of the Malformation Complex in Correlation With the Genotype in Patients With Robinow Syndrome: Review ArticleAli Al Kaissi, Vladimir Kenis, Mohammad Shboul, et al.
Medicines (Basel, Switzerland)|June 1, 2019
Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT ScanAli Al Kaissi, Mohammad Shboul, Vladimir Kenis, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|July 28, 2025
Whole-exome sequencing for prenatal diagnosis of fetal anomalies: insights from a Jordanian cohortMohammad Shboul, Nadia Badaro, Reem Darweesh, et al.
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