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JBCGenetics. Year: 2020, Volume: 3, Issue: 2

    Editorial

  1. Dual genetic diagnoses - underappreciated "double trouble"
    Christian Beetz, Peter Bauer
    JBCGenetics. 2020; 3(2): 52-53
    » Abstract » PDF» doi: 10.24911/JBCGenetics/183-1600154983

  2. Original Research (Original Article)

  3. Genetic and clinical approach to macrocephaly: a 5-year single-center study
    Muhsin Elmas, Umit Can Yildirim
    JBCGenetics. 2020; 3(2): 54-59
    » Abstract » PDF» doi: 10.24911/JBCGenetics/183-1594283408

  4. Role of religion/spirituality in the context of genetic counseling: health professionals' experiences in an Islamic country
    Khadijah Bakur, Jumana Al-Aama, Zuhair Alhassnan, Helen Brooks, Tara Clancy, Saud Takroni, Fiona Ulph
    JBCGenetics. 2020; 3(2): 60-70
    » Abstract » PDF» doi: 10.24911/JBCGenetics/183-1596638212

  5. Association of vitamin D receptor gene fok1 polymorphism with bone health in Pakistani population
    Najam Farooq, Anwar Ullah, Abida Arshad, Navida Riaz, Jabar Zaman Khan, Sobia Tabassum, Muhammad Arshad Malik
    JBCGenetics. 2020; 3(2): 71-76
    » Abstract » PDF» doi: 10.24911/JBCGenetics/183-1588174375

  6. Review Article

  7. Molecular testing approaches in thyroid cancer diagnosis
    Abdul-Mohsen Gaeth AlHejaily, Naji Jamil AlJohani
    JBCGenetics. 2020; 3(2): 77-83
    » Abstract » PDF» doi: 10.24911/JBCGenetics/183-1594975192

  8. Peculiar, poorly known, rare congenital bleeding disorders presenting thrombotic events: an understudied chapter of molecular, blood coagulation defects
    Antonio Girolami, Elisabetta Cosi, Silvia Ferrari, Claudia Santarossa, Bruno Girolami
    JBCGenetics. 2020; 3(2): 84-93
    » Abstract » PDF» doi: 10.24911/JBCGenetics/183-1592295836

  9. Prevention of hemoglobinopathies in Saudi Arabia: efficacy of national premarital screening and the feasibility of preimplantation genetic diagnosis
    Muhammad Umair, Majid Alfadhel
    JBCGenetics. 2020; 3(2): 94-99
    » Abstract » PDF» doi: 10.24911/JBCGenetics/183-1595487640

  10. Case Report

  11. Opsismodysplasia and Dilated Cardiomyopathy: a case report
    Muneer Almutairi, Mohammed Almannai
    JBCGenetics. 2020; 3(2): 100-103
    » Abstract » PDF» doi: 10.24911/JBCGenetics/183-1595951481

  12. A case of de novo microdeletion with combination of 1q21.1 and 14q32.2q32.31
    Hale Onder Yilmaz, Kadri Karaer, Orkun Yilmaz
    JBCGenetics. 2020; 3(2): 104-107
    » Abstract » PDF» doi: 10.24911/JBCGenetics/183-1592502000

  13. Infantile systemic hyalinosis: report of a case from Bahrain and review of literature
    Zahra Alsahlawi, Fatema Naser Alfayez, Sayed Mohamed Hasan, Deena Mohammed, Emtethal Aljishi
    JBCGenetics. 2020; 3(2): 108-112
    » Abstract » PDF» doi: 10.24911/JBCGenetics/183-1596702951

  14. Inherited Robertsonian translocation (13;14) in a child with Down's syndrome
    Srilekha Avvari, Neelu Mishra, Sujatha Madireddy, Venkateshwari Ananthapur
    JBCGenetics. 2020; 3(2): 113-117
    » Abstract » PDF» doi: 10.24911/JBCGenetics/183-1592993055