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1 . Academic Journal
Evaluating the association of missense mutations in cyclin E1 and MYC genes with breast cancer using computational analysis
저자
by
Aftab, Ayesha
;
Ahmad, Bashir
;
Mallah, Ghulam Ali
;
Hussain, Hafiz Muhammad Jafar
;
Dilshad, Aamna
, et al.
소스
In
Human Gene
December 2023 38
Full Text (ScienceDirect)
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7 . Academic Journal
A TOP6BL mutation abolishes meiotic DNA double-strand break formation and causes human infertility
저자
by
Jiao, Yuying
;
Fan, Suixing
;
Jabeen, Nazish
;
Zhang, Huan
;
Khan, Ranjha
, et al.
소스
In
Science Bulletin
30 December 2020 65(24):2120-2129
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7 . Academic Journal
Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseases.
저자
by
Brock, Daniel C
;
Wang, Meng
;
Hussain, Hafiz Muhammad Jafar
;
Rauch, David E
;
Marra, Molly
, et al.
소스
Human Molecular Genetics; Jun2024, Vol. 33 Issue 11, p945-957, 13p
Full Text (OUP)
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7 . Academic Journal
Novel cis compound heterozygous variants in MYO6 causes early onset of non-syndromic hearing loss in a Chinese family.
저자
by
Haiting Ji
;
Lichun Zhang
;
Hussain, Hafiz Muhammad Jafar
;
Aftab, Ayesha
;
Huiqian Yu
, et al.
소스
Frontiers in Genetics; 2024, p1-8, 8p
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7 . Academic Journal
Novel Pathogenic Mutations Identified from Whole-Genome Sequencing in Unsolved Cases of Patients Affected with Inherited Retinal Diseases.
저자
by
Hussain, Hafiz Muhammad Jafar
;
Wang, Meng
;
Huang, Austin
;
Schmidt, Ryan
;
Qian, Xinye
, et al.
소스
Genes
. Feb2023, Vol. 14 Issue 2, p447. 12p.
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7 . Academic Journal
RETRACTED: A graphene oxide-based hairpin probe coupling duplex-specific nuclease signal amplification for detection and imaging of mRNA in living cells
저자
by
Xu, Wei
;
Zhao, Aiwu
;
Zuo, Fangtao
;
Hussain, Hafiz Muhammad Jafar
.
소스
In
Talanta
1 April 2019 195:732-738
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6 . Academic Journal
Mutation in XPO5 causes adult-onset autosomal dominant familial focal segmental glomerulosclerosis.
저자
by
Hussain, Hafiz Muhammad Jafar
;
Cai, Yikai
;
Weng, Qinjie
;
Tong, Jun
;
Aftab, Ayesha
, et al.
소스
Human Genomics; 11/12/2022, Vol. 16 Issue 1, p1-12, 12p
Open Access (BioMed Central)
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7 . Academic Journal
Association between XRCC3 p.Thr241Met polymorphism and risk of glioma: A systematic review and meta-analysis.
저자
by
Tan, Shing Cheng
;
Low, Teck Yew
;
Hussain, Hafiz Muhammad Jafar
;
Sharzehan, Mohamad Ayub Khan
;
Sito, Hilary
, et al.
소스
PLoS ONE
. 10/20/2022, Vol. 17 Issue 10, p1-15. 15p.
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7 . Academic Journal
Novel homozygous variants in ATCAY, MCOLN1, and SACS in complex neurological disorders
저자
by
Manzoor, Humera
;
Brüggemann, Norbert
;
Hussain, Hafiz Muhammad Jafar
;
Bäumer, Tobias
;
Hinrichs, Frauke
, et al.
소스
In
Parkinsonism and Related Disorders
June 2018 51:91-95
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7 . Periodical
A biallelic variant of DCAF13implicated in a neuromuscular disorder in humans
저자
by
Manzoor, Humera
;
Zahid, Hafsa
;
Emerling, Christopher A.
;
Kumar, Kishore R.
;
Hussain, Hafiz Muhammad Jafar
, et al.
소스
European Journal of Human Genetics: EJHG; 20230101, Issue: Preprints p1-9, 9p
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