Bilal Azab

Publication Activity (10 Years)

Years Active: 2020-2022
Publications (10 Years): 8

Top Topics

Autism Spectrum Disorder

Intellectual Disability

Positron Emission Tomography

Top Venues

Congenital anomalies

Diagnostics (Basel, Switzerland)

The application of clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Mohamed Tawalbeh, Dunia Aburizeg, Bayan O Abu Alragheb, Wala Sami Alaqrabawi, Zain Dardas, Luma Srour, Baraah Hatem Altarayra, Ayman A Zayed, Zaid El Omari, Bilal Azab
SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and Management. Genes 13 (12) (2022)
Bilal Azab, Omar Rabab'h, Dunia Aburizeg, Hashim Mohammad, Zain Dardas, Lina Mustafa, Ruba A Khasawneh, Heyam Awad, Ma'mon M Hatmal, Eyad Altamimi
Potential Composite Digenic Contribution of NPC1 and NOD2 Leading to Atypical Lethal Niemann-Pick Type C with Initial Crohn's Disease-like Presentation: Genotype-Phenotype Correlation Study. Genes 13 (6) (2022)
Tareq Saleh, Ahmad Alhesa, Mohammed El-Sadoni, Nisreen Abu Shahin, Elham Alsharaiah, Sofian Al Shboul, Heyam Awad, Sarah Bloukh, Mahmoud Al-Balas, Mohammad Alsalem, Bilal Azab, Tariq N Al-Adily
The Expression of the Senescence-Associated Biomarker Lamin B1 in Human Breast Cancer. Diagnostics (Basel, Switzerland) 12 (3) (2022)
Mohamed Tawalbeh, Dunia Aburizeg, Bayan O Abu Alragheb, Wala Sami Alaqrabawi, Zain Dardas, Luma Srour, Baraah Hatem Altarayra, Ayman A Zayed, Zaid El Omari, Bilal Azab
SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and Management. Genes 13 (12) (2022)
Mohamed Tawalbeh, Dunia Aburizeg, Bayan O Abu Alragheb, Wala Sami Alaqrabawi, Zain Dardas, Luma Srour, Baraah Hatem Altarayra, Ayman A Zayed, Zaid El Omari, Bilal Azab
SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and Management. Genes 13 (12) (2022)
Mohamed Tawalbeh, Dunia Aburizeg, Bayan O Abu Alragheb, Wala Sami Alaqrabawi, Zain Dardas, Luma Srour, Baraah Hatem Altarayra, Ayman A Zayed, Zaid El Omari, Bilal Azab
SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and Management. Genes 13 (12) (2022)
Montaha M Al-Iede, Mariam Khanfar, Luma Srour, Raja Rabah, Mousa A Al-Abbadi, Bilal Azab, Eman Farouk Badran
A homozygous variant in ABCA3 is associated with severe respiratory distress and early neonatal death. Congenital anomalies 61 (6) (2021)
Eyad Altamimi, Mariam Khanfar, Omar Rabab'h, Zain Dardas, Luma Srour, Lina Mustafa, Bilal Azab
Effect of Genetic Testing on Diagnosing Gastrointestinal Pediatric Patients with Previously Undiagnosed Diseases. The application of clinical genetics 13 (2020)