E-ISSN 1658-8088 | ISSN 1658-807X
 

Original Article 



How to Cite this Article
Pubmed Style

Alduaiji R, Alqahtani L, Alqadiri R, Alotaibi L, abolfotouh M, Alfadhel M. Opinion of geneticist regarding performing preimplantation genetic testing for monogenic disorder for variants of unknown significance. JBCGenetics. 2023; 6(1): 36-40. doi:10.24911/JBCGenetics/183-1676870604


Web Style

Alduaiji R, Alqahtani L, Alqadiri R, Alotaibi L, abolfotouh M, Alfadhel M. Opinion of geneticist regarding performing preimplantation genetic testing for monogenic disorder for variants of unknown significance. https://www.jbcgenetics.com//?mno=144284 [Access: October 03, 2023]. doi:10.24911/JBCGenetics/183-1676870604


AMA (American Medical Association) Style

Alduaiji R, Alqahtani L, Alqadiri R, Alotaibi L, abolfotouh M, Alfadhel M. Opinion of geneticist regarding performing preimplantation genetic testing for monogenic disorder for variants of unknown significance. JBCGenetics. 2023; 6(1): 36-40. doi:10.24911/JBCGenetics/183-1676870604



Vancouver/ICMJE Style

Alduaiji R, Alqahtani L, Alqadiri R, Alotaibi L, abolfotouh M, Alfadhel M. Opinion of geneticist regarding performing preimplantation genetic testing for monogenic disorder for variants of unknown significance. JBCGenetics. (2023), [cited October 03, 2023]; 6(1): 36-40. doi:10.24911/JBCGenetics/183-1676870604



Harvard Style

Alduaiji, R., Alqahtani, . L., Alqadiri, . R., Alotaibi, . L., abolfotouh, . M. & Alfadhel, . M. (2023) Opinion of geneticist regarding performing preimplantation genetic testing for monogenic disorder for variants of unknown significance. JBCGenetics, 6 (1), 36-40. doi:10.24911/JBCGenetics/183-1676870604



Turabian Style

Alduaiji, Reema, Laila Alqahtani, Reema Alqadiri, Lena Alotaibi, Mostafa abolfotouh, and Majid Alfadhel. 2023. Opinion of geneticist regarding performing preimplantation genetic testing for monogenic disorder for variants of unknown significance. Journal of Biochemical and Clinical Genetics, 6 (1), 36-40. doi:10.24911/JBCGenetics/183-1676870604



Chicago Style

Alduaiji, Reema, Laila Alqahtani, Reema Alqadiri, Lena Alotaibi, Mostafa abolfotouh, and Majid Alfadhel. "Opinion of geneticist regarding performing preimplantation genetic testing for monogenic disorder for variants of unknown significance." Journal of Biochemical and Clinical Genetics 6 (2023), 36-40. doi:10.24911/JBCGenetics/183-1676870604



MLA (The Modern Language Association) Style

Alduaiji, Reema, Laila Alqahtani, Reema Alqadiri, Lena Alotaibi, Mostafa abolfotouh, and Majid Alfadhel. "Opinion of geneticist regarding performing preimplantation genetic testing for monogenic disorder for variants of unknown significance." Journal of Biochemical and Clinical Genetics 6.1 (2023), 36-40. Print. doi:10.24911/JBCGenetics/183-1676870604



APA (American Psychological Association) Style

Alduaiji, R., Alqahtani, . L., Alqadiri, . R., Alotaibi, . L., abolfotouh, . M. & Alfadhel, . M. (2023) Opinion of geneticist regarding performing preimplantation genetic testing for monogenic disorder for variants of unknown significance. Journal of Biochemical and Clinical Genetics, 6 (1), 36-40. doi:10.24911/JBCGenetics/183-1676870604





Most Viewed 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
  • 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

  • Case report of 49, XXXXY syndrome: first case in Oman
    Musallam Said Al Araimi, Salwa Ali AlObaidani, Zainab Al Hashmi, Ruba Al Lawati, Hiba Al Mazrooai Al Mazrooai
    JBCGenetics. 2020; 3(1): 28-31
    » Abstract » doi: 10.24911/JBCGenetics/183-1584426923

  • Most Cited Articles