| Case Report Online Publishing Date: | ||
JBCGenetics. 2019; 2(1): 70-73 | ||
| How to Cite this Article |
| Pubmed Style Almannai M, Althunayyan W, Alamin M, Rendeiro P, Tashkandi S. A case report of de novo 11q triplication, duplication, and segmental area of absence of heterozygosity in an infant with dysmorphic features, failure to thrive, and developmental delay.. JBCGenetics. 2019; 2(1): 70-73. doi:10.24911/JBCGenetics/183-1547056081 Web Style Almannai M, Althunayyan W, Alamin M, Rendeiro P, Tashkandi S. A case report of de novo 11q triplication, duplication, and segmental area of absence of heterozygosity in an infant with dysmorphic features, failure to thrive, and developmental delay.. https://www.jbcgenetics.com/?mno=25413 [Access: April 25, 2024]. doi:10.24911/JBCGenetics/183-1547056081 AMA (American Medical Association) Style Almannai M, Althunayyan W, Alamin M, Rendeiro P, Tashkandi S. A case report of de novo 11q triplication, duplication, and segmental area of absence of heterozygosity in an infant with dysmorphic features, failure to thrive, and developmental delay.. JBCGenetics. 2019; 2(1): 70-73. doi:10.24911/JBCGenetics/183-1547056081 Vancouver/ICMJE Style Almannai M, Althunayyan W, Alamin M, Rendeiro P, Tashkandi S. A case report of de novo 11q triplication, duplication, and segmental area of absence of heterozygosity in an infant with dysmorphic features, failure to thrive, and developmental delay.. JBCGenetics. (2019), [cited April 25, 2024]; 2(1): 70-73. doi:10.24911/JBCGenetics/183-1547056081 Harvard Style Almannai, M., Althunayyan, . W., Alamin, . M., Rendeiro, . P. & Tashkandi, . S. (2019) A case report of de novo 11q triplication, duplication, and segmental area of absence of heterozygosity in an infant with dysmorphic features, failure to thrive, and developmental delay.. JBCGenetics, 2 (1), 70-73. doi:10.24911/JBCGenetics/183-1547056081 Turabian Style Almannai, Mohammed, Walaa Althunayyan, Mohammed Alamin, Paula Rendeiro, and Suha Tashkandi. 2019. A case report of de novo 11q triplication, duplication, and segmental area of absence of heterozygosity in an infant with dysmorphic features, failure to thrive, and developmental delay.. Journal of Biochemical and Clinical Genetics, 2 (1), 70-73. doi:10.24911/JBCGenetics/183-1547056081 Chicago Style Almannai, Mohammed, Walaa Althunayyan, Mohammed Alamin, Paula Rendeiro, and Suha Tashkandi. "A case report of de novo 11q triplication, duplication, and segmental area of absence of heterozygosity in an infant with dysmorphic features, failure to thrive, and developmental delay.." Journal of Biochemical and Clinical Genetics 2 (2019), 70-73. doi:10.24911/JBCGenetics/183-1547056081 MLA (The Modern Language Association) Style Almannai, Mohammed, Walaa Althunayyan, Mohammed Alamin, Paula Rendeiro, and Suha Tashkandi. "A case report of de novo 11q triplication, duplication, and segmental area of absence of heterozygosity in an infant with dysmorphic features, failure to thrive, and developmental delay.." Journal of Biochemical and Clinical Genetics 2.1 (2019), 70-73. Print. doi:10.24911/JBCGenetics/183-1547056081 APA (American Psychological Association) Style Almannai, M., Althunayyan, . W., Alamin, . M., Rendeiro, . P. & Tashkandi, . S. (2019) A case report of de novo 11q triplication, duplication, and segmental area of absence of heterozygosity in an infant with dysmorphic features, failure to thrive, and developmental delay.. Journal of Biochemical and Clinical Genetics, 2 (1), 70-73. doi:10.24911/JBCGenetics/183-1547056081 |
Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Muhammad Arshad
JBCGenetics. 2018; 1(2): 66-76
» Abstract » doi: 10.24911/JBCGenetics/183-1530765389
Saleh Alghamdi, Sarah Alkwai, Mohammad Ilyas
JBCGenetics. 2018; 1(1): 2-9
» Abstract » doi: 10.24911/JBCGenetics/183-1531548689
Lamia Alsubaie, Saeed Alturki, Ali Alothaim, Ahmed Alfares
JBCGenetics. 2018; 1(1): 31-36
» Abstract » doi: 10.24911/JBCGenetics/183-1529928114
AlAnoud Al-Jarbou, Afnan Al-Turki, Suha Tashkandi, Eissa A. Faqeih
JBCGenetics. 2018; 1(1): 37-39
» Abstract » doi: 10.24911/JBCGenetics/183-1530040885
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
Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Muhammad Arshad
JBCGenetics. 2018; 1(2): 66-76
» Abstract » doi: 10.24911/JBCGenetics/183-1530765389
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
Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Safdar Abbas
JBCGenetics. 2018; 1(1): 10-18
» Abstract » doi: 10.24911/JBCGenetics/183-1532177257
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
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
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]
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]
Ahmed Alfares,
JBCGenetics. 2018; 1(2): 51-52
» Abstract » doi: 10.24911/JBCGenetics/183-1546945268
Cited : 4 times [Click to see citing articles]
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]
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]
| |
About Journal of Biochemical and Clinical GeneticsThe Journal of Biochemical and Clinical Genetics (JBCGenetics) is a peer-reviewed, open access medical journal. Owner: Saudi Society of Medical ... Read more. For best results, please use Internet Explorer or Google Chrome. |
Contact InformationTitle Owner: Saudi Society of Medical Genetics Society Email: info@ssmg.org.sa Editor in Chief: dralfadhelm@jbcgenetics.com Contact the publisher: contact@discoverpublish.com Publisher: Discover STM Publishing Ltd, 82 Leslie's Arch, Old Quarter, Ballincollig, Cork, P31 RY62, Ireland. Hours: M-F: 8:30am - 5:30pm Contact Emails: Journal Editorial Office: contact@jbcgenetics.com Billing Support: contact@discoverpublish.com Technical Support: |
