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Azage, Meron
15
results:
Search for persons
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Format
Online (15)
Mediatypes
Articles (Online) (10)
OpenAccess-fulltext (5)
Sorted by: Relevance
Sorted by: Year
?
1
Disparities in Genetic Testing for Neurologic Disorders:
Baldwin, Aaron
;
Copeland, Juliette
;
Azage, Meron
...
Neurology. 102 (2024) 6 - p. , 2024
Link:
https://doi.org/10.1212/..
?
2
P203: Genetic testing in an adult neuromuscular clinic: Dia..:
Johnson, Kelsey
;
Azage, Meron
;
Babaian, Nareen
...
Genetics in Medicine Open. 1 (2023) 1 - p. 100231 , 2023
Link:
https://doi.org/10.1016/..
?
3
Genetic testing in adults with neurologic disorders: indica..:
Dratch, Laynie
;
Azage, Meron
;
Baldwin, Aaron
...
Journal of Neurology. 271 (2023) 2 - p. 733-747 , 2023
Link:
https://doi.org/10.1007/..
?
4
Preimplantation Genetic Testing for Adult-Onset Neurodegene..:
Paul, Rachel A.
;
Baldwin, Aaron
;
Johnson, Kelsey
...
Neurology. 101 (2023) 19 - p. 836-841 , 2023
Link:
https://doi.org/10.1212/..
?
5
De novo heterozygous missense and loss‐of‐function variants..:
Chilton, Ilana
;
Okur, Volkan
;
Vitiello, Giuseppina
...
American Journal of Medical Genetics Part A. 182 (2020) 5 - p. 962-973 , 2020
Link:
https://doi.org/10.1002/..
?
6
Pathogenic WDFY3 variants cause neurodevelopmental disorder..:
Le Duc, Diana
;
Giulivi, Cecilia
;
Hiatt, Susan M
...
Brain. 142 (2019) 9 - p. 2617-2630 , 2019
Link:
https://doi.org/10.1093/..
?
7
De novo mutations in CSNK2A1 are associated with neurodevel..:
Okur, Volkan
;
Cho, Megan T.
;
Henderson, Lindsay
...
Human Genetics. 135 (2016) 7 - p. 699-705 , 2016
Link:
https://doi.org/10.1007/..
?
8
Five patients with a chromosome 1q21.1 triplication show ma..:
Van Dijck, Anke
;
van der Werf, Ilse M.
;
Reyniers, Edwin
...
European Journal of Medical Genetics. 58 (2015) 10 - p. 503-508 , 2015
Link:
https://doi.org/10.1016/..
?
9
A novel maternally inherited 8q24.3 and a rare paternally i..:
Hu, Jie
;
Sathanoori, Malini
;
Kochmar, Sally
...
American Journal of Medical Genetics Part A. 167 (2015) 8 - p. 1921-1926 , 2015
Link:
https://doi.org/10.1002/..
?
10
Mutations in ZBTB20 cause Primrose syndrome:
Cordeddu, Viviana
;
Redeker, Bert
;
Stellacci, Emilia
...
Nature Genetics. 46 (2014) 8 - p. 815-817 , 2014
Link:
https://doi.org/10.1038/..
?
11
Pathogenic WDFY3 variants cause neurodevelopmental disorder..:
Le Duc, Diana
;
Giulivi, Cecilia
;
Hiatt, Susan M
...
qt5n82c4vr. , 2019
Link:
https://escholarship.org..
?
12
Pathogenic WDFY3 variants cause neurodevelopmental disorder..:
Le Duc, Diana
;
Giulivi, Cecilia
;
Hiatt, Susan M
...
qt8pr0p6tk. , 2019
Link:
https://escholarship.org..
?
13
Pathogenic WDFY3 variants cause neurodevelopmental disorder..:
Le Duc, Diana
;
Giulivi, Cecilia
;
Hiatt, Susan M
...
qt8cc843ht. , 2019
Link:
https://escholarship.org..
?
14
Missense variants in the chromatin remodeler CHD1 are assoc..:
Pilarowski, Genay O
;
Vernon, Hilary J
;
Applegate, Carolyn D
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834353/. , 2017
Link:
http://www.ncbi.nlm.nih...
?
15
P203: Genetic testing in an adult neuromuscular clinic: Dia..:
Kelsey Johnson
;
Meron Azage
;
Nareen Babaian
...
http://www.sciencedirect.com/science/article/pii/S2949774423002315. , 2023
Link:
https://doi.org/10.1016/..
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