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Mohammed, Inaam N.
97
results:
Search for persons
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Online (97)
Mediatypes
Articles (Online) (69)
Bookchapter (Online) (2)
OpenAccess-fulltext (26)
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?
1
Bi-allelic PRRT2 variants may predispose to Self-limited Fa..:
Koko, Mahmoud
;
Elseed, Maha A.
;
Mohammed, Inaam N.
...
European Journal of Human Genetics. , 2024
Link:
https://doi.org/10.1038/..
?
2
Case Report: A New Family With Pontocerebellar Hypoplasia 1..:
Amin, Mutaz
;
Vignal, Cedric
;
Hamed, Ahlam A. A.
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
3
Genetic diagnosis in Sudanese and Tunisian families with sy..:
Yahia, Ashraf
;
Ayed, Ikhlas Ben
;
Hamed, Ahlam A.
...
Annals of Human Genetics. 86 (2022) 4 - p. 181-194 , 2022
Link:
https://doi.org/10.1111/..
?
4
A novel homozygous mutation in TRAPPC9 gene causing autosom..:
Amin, Mutaz
;
Vignal, Cedric
;
Eltaraifee, Esraa
...
BMC Medical Genomics. 15 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
5
Novel variants causing megalencephalic leukodystrophy in Su..:
Amin, Mutaz
;
Vignal, Cedric
;
Hamed, Ahlam A. A.
...
Journal of Human Genetics. 67 (2021) 3 - p. 127-132 , 2021
Link:
https://doi.org/10.1038/..
?
6
Pathogenic Variants in ABHD16A Cause a Novel Psychomotor De..:
Yahia, Ashraf
;
Elsayed, Liena E. O.
;
Valter, Remi
...
Frontiers in Neurology. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
7
An identical‐by‐descent novel splice‐donor variant inPRUNE1..:
Koko, Mahmoud
;
Yahia, Ashraf
;
Elsayed, Liena E.
...
Annals of Human Genetics. 85 (2021) 5 - p. 186-195 , 2021
Link:
https://doi.org/10.1111/..
?
8
Novel Homozygous Missense Mutation in the ARG1 Gene in a La..:
Elsayed, Liena E. O.
;
Mohammed, Inaam N.
;
Hamed, Ahlam A. A.
...
Frontiers in Neurology. 11 (2020) - p. , 2020
Link:
https://doi.org/10.3389/..
?
9
Case report of a novel homozygous splice site mutation in P..:
Elsayed, Liena E. O.
;
Mohammed, Inaam N.
;
Hamed, Ahlam A. A.
...
BMC Medical Genetics. 19 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
10
Research: Prevalence of neural tube defects Khartoum, Sudan..:
Omer, Ilham M.
;
Abdullah, Osman M.
;
Mohammed, Inaam N.
.
BMC Research Notes. 9 (2016) 1 - p. , 2016
Link:
https://doi.org/10.1186/..
?
11
Hereditary spastic paraplegias: identification of a novel S..:
Elsayed, Liena E O
;
Mohammed, Inaam N
;
Hamed, Ahlam A A
...
European Journal of Human Genetics. 25 (2016) 1 - p. 100-110 , 2016
Link:
https://doi.org/10.1038/..
?
12
A Novel Nonsense Mutation in DNAJC6Expands the Phenotype of..:
Elsayed, Liena Elbaghir Omer
;
Drouet, Valérie
;
Usenko, Tatiana
...
Annals of Neurology. 79 (2016) 2 - p. 335-337 , 2016
Link:
https://doi.org/10.1002/..
?
13
Case Report: A New Family With Pontocerebellar Hypoplasia 1..:
Amin, Mutaz
;
Vignal, Cedric
;
Hamed, Ahlam A. A
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201487/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
14
A novel homozygous mutation in TRAPPC9 gene causing autosom..:
Amin, Mutaz
;
Vignal, Cedric
;
Eltaraifee, Esraa
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644490/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
15
Pathogenic Variants in ABHD16A Cause a Novel Psychomotor De..:
Yahia, Ashraf
;
Elsayed, Liena E. O
;
Valter, Remi
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8417901/. , 2021
Link:
http://www.ncbi.nlm.nih...
1-15