E-ISSN 1658-8088 | ISSN 1658-807X
 

Original Article

Online Publishing Date:
28 / 03 / 2023

 



How to Cite this Article
Pubmed Style

AlMaarik B, Aloraini T, Paclejan R, Balwi M, Alsubaie L, Alswaid A, Eyiad W, Mutairi FA, Ababneh F, Alfadhel M, Alfares AA. Supplementary testing after negative or inconclusive exome sequencing results. JBCGenetics. 2023; 6(1): 1-13. doi:10.24911/JBCGenetics/183-1659513785


Web Style

AlMaarik B, Aloraini T, Paclejan R, Balwi M, Alsubaie L, Alswaid A, Eyiad W, Mutairi FA, Ababneh F, Alfadhel M, Alfares AA. Supplementary testing after negative or inconclusive exome sequencing results. https://www.jbcgenetics.com/?mno=95398 [Access: July 12, 2024]. doi:10.24911/JBCGenetics/183-1659513785


AMA (American Medical Association) Style

AlMaarik B, Aloraini T, Paclejan R, Balwi M, Alsubaie L, Alswaid A, Eyiad W, Mutairi FA, Ababneh F, Alfadhel M, Alfares AA. Supplementary testing after negative or inconclusive exome sequencing results. JBCGenetics. 2023; 6(1): 1-13. doi:10.24911/JBCGenetics/183-1659513785



Vancouver/ICMJE Style

AlMaarik B, Aloraini T, Paclejan R, Balwi M, Alsubaie L, Alswaid A, Eyiad W, Mutairi FA, Ababneh F, Alfadhel M, Alfares AA. Supplementary testing after negative or inconclusive exome sequencing results. JBCGenetics. (2023), [cited July 12, 2024]; 6(1): 1-13. doi:10.24911/JBCGenetics/183-1659513785



Harvard Style

AlMaarik, B., Aloraini, . T., Paclejan, . R., Balwi, . M., Alsubaie, . L., Alswaid, . A., Eyiad, . W., Mutairi, . F. A., Ababneh, . F., Alfadhel, . M. & Alfares, . A. A. (2023) Supplementary testing after negative or inconclusive exome sequencing results. JBCGenetics, 6 (1), 1-13. doi:10.24911/JBCGenetics/183-1659513785



Turabian Style

AlMaarik, Balsam, Taghrid Aloraini, Roselyn Paclejan, Mohammed Balwi, Lamia Alsubaie, Abdulrahman Alswaid, Wafaa Eyiad, Fuad Al Mutairi, Faroug Ababneh, Majid Alfadhel, and Ahmed A. Alfares. 2023. Supplementary testing after negative or inconclusive exome sequencing results. Journal of Biochemical and Clinical Genetics, 6 (1), 1-13. doi:10.24911/JBCGenetics/183-1659513785



Chicago Style

AlMaarik, Balsam, Taghrid Aloraini, Roselyn Paclejan, Mohammed Balwi, Lamia Alsubaie, Abdulrahman Alswaid, Wafaa Eyiad, Fuad Al Mutairi, Faroug Ababneh, Majid Alfadhel, and Ahmed A. Alfares. "Supplementary testing after negative or inconclusive exome sequencing results." Journal of Biochemical and Clinical Genetics 6 (2023), 1-13. doi:10.24911/JBCGenetics/183-1659513785



MLA (The Modern Language Association) Style

AlMaarik, Balsam, Taghrid Aloraini, Roselyn Paclejan, Mohammed Balwi, Lamia Alsubaie, Abdulrahman Alswaid, Wafaa Eyiad, Fuad Al Mutairi, Faroug Ababneh, Majid Alfadhel, and Ahmed A. Alfares. "Supplementary testing after negative or inconclusive exome sequencing results." Journal of Biochemical and Clinical Genetics 6.1 (2023), 1-13. Print. doi:10.24911/JBCGenetics/183-1659513785



APA (American Psychological Association) Style

AlMaarik, B., Aloraini, . T., Paclejan, . R., Balwi, . M., Alsubaie, . L., Alswaid, . A., Eyiad, . W., Mutairi, . F. A., Ababneh, . F., Alfadhel, . M. & Alfares, . A. A. (2023) Supplementary testing after negative or inconclusive exome sequencing results. Journal of Biochemical and Clinical Genetics, 6 (1), 1-13. doi:10.24911/JBCGenetics/183-1659513785





Most Viewed Articles
Most Accessed Articles

  • Frontonasal dysplasia: a review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Muhammad Arshad
    JBCGenetics. 2018; 1(2): 66-76
    » Abstract » doi: 10.24911/JBCGenetics/183-1530765389

  • The role of C-terminal tensin-like (Cten) gene in cancer metastasis
    Saleh Alghamdi, Sarah Alkwai, Mohammad Ilyas
    JBCGenetics. 2018; 1(1): 2-9
    » Abstract » doi: 10.24911/JBCGenetics/183-1531548689

  • Clinical reassessment of post-laboratory variant call format (VCF) files
    Lamia Alsubaie, Saeed Alturki, Ali Alothaim, Ahmed Alfares
    JBCGenetics. 2018; 1(1): 31-36
    » Abstract » doi: 10.24911/JBCGenetics/183-1529928114

  • Microcephalic osteodysplastic primordial dwarfism type II and Klinefelter syndrome: report of two competing growth syndromes
    AlAnoud Al-Jarbou, Afnan Al-Turki, Suha Tashkandi, Eissa A. Faqeih
    JBCGenetics. 2018; 1(1): 37-39
    » Abstract » doi: 10.24911/JBCGenetics/183-1530040885

  • Recessive ARFGEF2 mutation causes progressive microcephaly, epilepsy, and a distinct MRI pattern
    Maram Alojair, Abdulaziz Alghamdi, Kalthoum Tlili, Sateesh Maddirevula, Fowzan Sami Alkuraya, Brahim Tabarki
    JBCGenetics. 2018; 1(1): 40-42
    » Abstract » doi: 10.24911/JBCGenetics/183-1531469195

  • Most Downloaded
    Top Downloaded Articles

  • Frontonasal dysplasia: a review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Muhammad Arshad
    JBCGenetics. 2018; 1(2): 66-76
    » Abstract » doi: 10.24911/JBCGenetics/183-1530765389

  • Generation of a mouse model of Primary Hyperoxaluria Type 1 via CRISPR/Cas9 mediated gene editing
    Kimberly A Coughlan, Rajanikanth J Maganti, Andrea Frassetto, Christine M DeAntonis, meredith Wolfrom, Anne-Renee Graham, Shawn M Hillier, Steven Fortucci, Hoor Al Jandal, Sue-Jean Hong, Paloma H Giangrande, Paolo GV Martini,
    JBCGenetics. 2019; 2(1): 28-39
    » Abstract » doi: 10.24911/JBCGenetics/183-1542047633

  • Syndactyly genes and classification: a mini review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Safdar Abbas
    JBCGenetics. 2018; 1(1): 10-18
    » Abstract » doi: 10.24911/JBCGenetics/183-1532177257

  • Recessive ARFGEF2 mutation causes progressive microcephaly, epilepsy, and a distinct MRI pattern
    Maram Alojair, Abdulaziz Alghamdi, Kalthoum Tlili, Sateesh Maddirevula, Fowzan Sami Alkuraya, Brahim Tabarki
    JBCGenetics. 2018; 1(1): 40-42
    » Abstract » doi: 10.24911/JBCGenetics/183-1531469195

  • Consanguinity, awareness, and genetic disorders among female university students in Riyadh, Saudi Arabia
    Hadil Alahdal, Huda Alshanbari, Hana Saud Almazroa, Sarah Majed Alayesh, Alaa Mohammad Alrhaili, Nora Alqubi, Fai Fahad Alzamil, Reem Albassam
    JBCGenetics. 2021; 4(1): 27-34
    » Abstract » doi: 10.24911/JBCGenetics/183-1601264923

  • Most Cited Articles
    Most Cited Articles

  • Frontonasal dysplasia: a review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Muhammad Arshad
    JBCGenetics. 2018; 1(2): 66-76
    » Abstract » doi: 10.24911/JBCGenetics/183-1530765389
    Cited : 4 times [Click to see citing articles]

  • Syndactyly genes and classification: a mini review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Safdar Abbas
    JBCGenetics. 2018; 1(1): 10-18
    » Abstract » doi: 10.24911/JBCGenetics/183-1532177257
    Cited : 4 times [Click to see citing articles]

  • Genomics in Saudi Arabia Call for Data-Sharing Policy
    Ahmed Alfares,
    JBCGenetics. 2018; 1(2): 51-52
    » Abstract » doi: 10.24911/JBCGenetics/183-1546945268
    Cited : 4 times [Click to see citing articles]

  • Consanguinity, awareness, and genetic disorders among female university students in Riyadh, Saudi Arabia
    Hadil Alahdal, Huda Alshanbari, Hana Saud Almazroa, Sarah Majed Alayesh, Alaa Mohammad Alrhaili, Nora Alqubi, Fai Fahad Alzamil, Reem Albassam
    JBCGenetics. 2021; 4(1): 27-34
    » Abstract » doi: 10.24911/JBCGenetics/183-1601264923
    Cited : 2 times [Click to see citing articles]

  • Harel-Yoon syndrome: the first case report from Saudi Arabia
    Alaa AlAyed, Manar A. Samman, Abdul Ali Peer-Zada, Mohammed Almannai
    JBCGenetics. 2020; 3(1): 22-27
    » Abstract » doi: 10.24911/JBCGenetics/183-1585816398
    Cited : 2 times [Click to see citing articles]