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Sadaf, Memoona
13
results:
Search for persons
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Format
Online (13)
Mediatypes
Articles (Online) (8)
OpenAccess-fulltext (5)
Sorted by: Relevance
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?
1
A novel framework for detection and prevention of denial of..:
Sadaf, Memoona
;
Iqbal, Zafar
;
Anwar, Zahid
...
Vehicular Communications. 46 (2024) - p. 100741 , 2024
Link:
https://doi.org/10.1016/..
?
2
Connected and Automated Vehicles: Infrastructure, Applicati..:
Sadaf, Memoona
;
Iqbal, Zafar
;
Javed, Abdul Rehman
...
Technologies. 11 (2023) 5 - p. 117 , 2023
Link:
https://doi.org/10.3390/..
?
3
Connected and Automated Vehicles: Infrastructure, Applicati..:
Memoona Sadaf
;
Zafar Iqbal
;
Abdul Rehman Javed
...
https://www.mdpi.com/2227-7080/11/5/117. , 2023
Link:
https://doi.org/10.3390/..
?
4
Connected and Automated Vehicles: Infrastructure, Applicati..:
Memoona Sadaf
;
Zafar Iqbal
;
Abdul Rehman Javed
...
Information and Communication Technologies. , 2023
Link:
https://doi.org/10.3390/..
?
5
Epigenetically dysregulated NOTCH-Delta-HES signaling casca..:
Hussan, Syeda Saliah
;
Ali, Muhammad Shrafat
;
Fatima, Mishal
..
Annals of Hematology. 103 (2023) 2 - p. 511-523 , 2023
Link:
https://doi.org/10.1007/..
?
6
Variants of humanCLDN9cause mild to profound hearing loss:
Ramzan, Memoona
;
Philippe, Christophe
;
Belyantseva, Inna A.
...
Human Mutation. 42 (2021) 10 - p. 1321-1335 , 2021
Link:
https://doi.org/10.1002/..
?
7
RIN2 and BBS7 variants as cause of a coincidental syndrome:
Shaukat, Memoona
;
Ishaq, Tayyaba
;
Muhammad, Niaz
.
European Journal of Medical Genetics. 63 (2020) 3 - p. 103755 , 2020
Link:
https://doi.org/10.1016/..
?
8
Spectrum of genetic variants in moderate to severe sporadic..:
Ramzan, Memoona
;
Bashir, Rasheeda
;
Salman, Midhat
...
Scientific Reports. 10 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/..
?
9
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset ..:
Ramzan, Memoona
;
Idrees, Hafiza
;
Mujtaba, Ghulam
...
Gene. 705 (2019) - p. 109-112 , 2019
Link:
https://doi.org/10.1016/..
?
10
A cornucopia of screening and diagnostic techniques for hum..:
Ramzan, Memoona
;
Ain, Noor ul
;
Ilyas, Sadaf
...
Journal of Virological Methods. 222 (2015) - p. 192-201 , 2015
Link:
https://doi.org/10.1016/..
?
11
Spectrum of genetic variants in moderate to severe sporadic..:
Ramzan, Memoona
;
Bashir, Rasheeda
;
Salman, Midhat
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368073/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
12
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset ..:
Ramzan, Memoona
;
Idrees, Hafiza
;
Mujtaba, Ghulam
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709079/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
13
Genetic causes of moderate to severe hearing loss point to ..:
Naz, Sadaf
;
Imtiaz, Ayesha
;
Mujtaba, Ghulam
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365349/. , 2016
Link:
http://www.ncbi.nlm.nih...
1-13
