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Abdulkareem, Angham Abdulrhman
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Online (56)
Mediatypes
Articles (Online) (38)
OpenAccess-fulltext (18)
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1
Unveiling genetics of non-syndromic albinism using whole ex..:
Zaman, Qaiser
;
Khan, Jamshid
;
Ahmad, Mashal
...
Gene. 894 (2024) - p. 147986 , 2024
Link:
https://doi.org/10.1016/..
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2
Two novel homozygous variants of ATP6V0A2 and ALDH18A1 lead..:
Zaman, Qaiser
;
Iftikhar, Aiman
;
Rehman, Gauhar
...
The Journal of Gene Medicine. 25 (2023) 10 - p. , 2023
Link:
https://doi.org/10.1002/..
?
3
Combinatorial Therapeutic Potential of Stem Cells and Benzi..:
Iqbal, Maryam
;
Shams, Sulaiman
;
Rafiq, Huma
...
Pharmaceuticals. 16 (2023) 2 - p. 306 , 2023
Link:
https://doi.org/10.3390/..
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4
A novel homozygous splice donor variant in the LRPPRC gene ..:
Muthaffar, Osama Y.
;
Abdulkareem, Angham Abdulrhman
;
Ashi, Abrar
.
Frontiers in Pediatrics. 11 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
5
Whole Exome Sequencing Reveals a Novel Homozygous Variant i..:
Abdulkareem, Angham Abdulrhman
;
Shirah, Bader H.
;
Naseer, Muhammad Imran
Genes. 14 (2023) 2 - p. 354 , 2023
Link:
https://doi.org/10.3390/..
?
6
Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot–..:
Zaman, Qaiser
;
Khan, Muhammad Abbas
;
Sahar, Kalsoom
...
Genes. 14 (2023) 2 - p. 328 , 2023
Link:
https://doi.org/10.3390/..
?
7
A Novel Homozygous Nonsense Variant in the DYM Underlies Dy..:
Bakar, Abu
;
Shams, Sulaiman
;
Bibi, Nousheen
...
Genes. 14 (2023) 2 - p. 510 , 2023
Link:
https://doi.org/10.3390/..
?
8
Whole exome sequencing identified five novel variants in CN..:
Abdulkareem, Angham Abdulrhman
;
Zaman, Qaiser
;
Khan, Hamza
...
Frontiers in Genetics. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
9
Phenotypic Classification of Eye Colour and Developmental V..:
Rahat, Murad Ali
;
Akbar, Fazal
;
Rasool, Akhtar
...
Biomedicines. 11 (2023) 4 - p. 1228 , 2023
Link:
https://doi.org/10.3390/..
?
10
Clinical whole exome sequencing revealed de novo heterozygo..:
Naseer, Muhammad Imran
;
Abdulkareem, Angham Abdulrhman
;
Rasool, Mahmood
...
Saudi Journal of Biological Sciences. 29 (2022) 7 - p. 103309 , 2022
Link:
https://doi.org/10.1016/..
?
11
Autosomal Recessive Spastic Paraplegia Type 78 Associated w..:
Algahtani, Hussein
;
Shirah, Bader
;
Alshammari, Salem
...
Movement Disorders Clinical Practice. 9 (2022) 7 - p. 997-1002 , 2022
Link:
https://doi.org/10.1002/..
?
12
Whole-Exome Sequencing Identifies Novel SCN1A and CACNB4 Ge..:
Naseer, Muhammad Imran
;
Abdulkareem, Angham Abdulrhman
;
Rasool, Mahmood
...
Frontiers in Pediatrics. 10 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
13
Novel variants in MPV17, PRX, GJB1, and SACS Cause Charcot–..:
Zaman, Qaiser
;
Khan, Muhammad Abbas
;
Sahar, Kalsoom
...
http://dx.doi.org/10.18725/OPARU-50867. , 2023
Link:
https://doi.org/10.18725..
?
14
Whole Exome Sequencing Reveals a Novel Homozygous Variant i..:
Angham Abdulrhman Abdulkareem
;
Bader H. Shirah
;
Muhammad Imran Naseer
https://www.mdpi.com/2073-4425/14/2/354. , 2023
Link:
https://doi.org/10.3390/..
?
15
A novel homozygous splice donor variant in the LRPPRC gene ..:
Osama Y. Muthaffar
;
Angham Abdulrhman Abdulkareem
;
Abrar Ashi
.
https://www.frontiersin.org/articles/10.3389/fped.2023.1288542/full. , 2023
Link:
https://doi.org/10.3389/..
1-15