E-ISSN 1658-8088 | ISSN 1658-807X
Digital Archiving & Preservation Policies
The published content is always valuable and like other scholarly publishers, Discover STM Publishing Ltd ensures that the published content is preserved properly in a systematic way, even if a journal stops publishing or the publisher is out of business.
To ensure preservation, Discover STM Publishing has made the following arrangements.
Routine website backups
We ensure at least one backup every 24 hours and a copy is stored at 3 different devices
Archiving with Discovery Services
We provide the content regularly to various discovery services and some of them include xml and fulltext-pdf files too. These discovery services are mentioned on each journal's website under Abstracting and Indexing link.
Permanent Preservation
We made arrangements with PORTICO that all content is available in case a journal ceases to publish or the publisher is out of business. PORTICO activates perpetual access rights when needed.
Most Viewed Articles
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Microcephalic osteodysplastic primordial dwarfism type II and Klinefelter syndrome: report of two competing growth syndromes
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» 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
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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
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» Abstract » doi: 10.24911/JBCGenetics/183-1584426923