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El‐Ruby, Mona
13
results:
Search for persons
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Format
Online (13)
Mediatypes
Articles (Online) (9)
OpenAccess-fulltext (4)
Sorted by: Relevance
Sorted by: Year
?
1
Chromosome 9p terminal deletion in nine Egyptian patients a..:
Mohamed, Amal M.
;
Kamel, Alaa K.
;
Eid, Maha M.
...
Molecular Genetics & Genomic Medicine. 9 (2021) 11 - p. , 2021
Link:
https://doi.org/10.1002/..
?
2
Advances in genomic diagnosis of a large cohort of Egyptian..:
Mazen, Inas
;
Mekkawy, Mona
;
Kamel, Alaa
...
American Journal of Medical Genetics Part A. 185 (2021) 6 - p. 1666-1677 , 2021
Link:
https://doi.org/10.1002/..
?
3
Identification of a novel homozygous ALX4 mutation in two u..:
El‐Ruby, Mona
;
El‐Din Fayez, Alaa
;
El‐Dessouky, Sara H.
...
American Journal of Medical Genetics Part A. 176 (2018) 5 - p. 1190-1194 , 2018
Link:
https://doi.org/10.1002/..
?
4
Clinical and molecular characterization of seven Egyptian f..:
Aglan, Mona
;
Amr, Khalda
;
Ismail, Samira
...
American Journal of Medical Genetics Part A. 167 (2015) 12 - p. 3054-3061 , 2015
Link:
https://doi.org/10.1002/..
?
5
Isodicentric Y chromosomes in Egyptian patients with disord..:
Mekkawy, Mona
;
Kamel, Alaa
;
El‐Ruby, Mona
...
American Journal of Medical Genetics Part A. 158A (2012) 7 - p. 1594-1603 , 2012
Link:
https://doi.org/10.1002/..
?
6
Blepharophimosis‐ptosis‐intellectual disability syndrome: A..:
Zaki, Maha S.
;
Otaify, Ghada A.
;
Ismail, Samira
...
American Journal of Medical Genetics Part A. 182 (2020) 12 - p. 2857-2866 , 2020
Link:
https://doi.org/10.1002/..
?
7
Muenke syndrome with pigmentary disorder and probable hemim..:
Abdel‐Salam, Ghada M. H.
;
Flores‐Sarnat, Laura
;
El‐Ruby, Mona O.
...
American Journal of Medical Genetics Part A. 155 (2010) 1 - p. 207-214 , 2010
Link:
https://doi.org/10.1002/..
?
8
Variable Associations of Klinefelter Syndrome in Children:
Mazen, Inas
;
El-Ruby, Mona
;
El-Bassyouni, Hala T.
Journal of Pediatric Endocrinology and Metabolism. 23 (2010) 10 - p. , 2010
Link:
https://doi.org/10.1515/..
?
9
Human variome project country nodes: Documenting genetic in..:
Patrinos, George P.
;
Smith, Timothy D.
;
Howard, Heather
...
Human Mutation. 33 (2012) 11 - p. 1513-1519 , 2012
Link:
https://doi.org/10.1002/..
?
10
Chromosome 9p terminal deletion in nine Egyptian patients a..:
Mohamed, Amal M
;
Kamel, Alaa K
;
Eid, Maha M
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606205/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
11
Chromosome 9p terminal deletion in nine Egyptian patients a..:
Amal M. Mohamed
;
Alaa K. Kamel
;
Maha M. Eid
...
https://doi.org/10.1002/mgg3.1829. , 2021
Link:
https://doi.org/10.1002/..
?
12
Turner syndrome in Diverse Populations:
Kruszka, Paul
;
Addissie, Yonit A
;
Tekendo-Ngongang, Cedrik
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8141514/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
13
Phenotypic characterization of rare interstitial deletion o..:
Ismail, Samira
;
Helmy, Nivine A
;
Mahmoud, Wael M
.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5020940/. , 2012
Link:
http://www.ncbi.nlm.nih...
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