Ich stimme zu, dass diese Seite Cookies verwende. Weitere Informationen finden Sie unter unseren Datenschutzerklärungen .
X
Salameh, Manar
11  Ergebnisse:
Personensuche X
?
1

Homozygous Knockout of Cep250 Leads to a Relatively Late-On..:

Abu-Diab, Alaa ; Gopalakrishnan, Prakadeeswari ; Matsevich, Chen...
Translational Vision Science & Technology.  12 (2023)  3 - p. 3 , 2023
Link: https://doi.org/10.1167/..
 
?
2

Whole genome sequencing for USH2A-associated disease reveal..:

Reurink, Janine ; Weisschuh, Nicole ; Garanto, Alejandro...
Human Genetics and Genomics Advances.  4 (2023)  2 - p. 100181 , 2023
Link: https://doi.org/10.1016/..
 
?
3

Gene augmentation therapy attenuates retinal degeneration i..:

Matsevich, Chen ; Gopalakrishnan, Prakadeeswari ; Chang, Ning...
Molecular Therapy.  31 (2023)  10 - p. 2948-2961 , 2023
Link: https://doi.org/10.1016/..
 
?
4

ABCA4c.859-25A>G, a Frequent Palestinian Founder Mutatio..:

Corradi, Zelia ; Salameh, Manar ; Khan, Mubeen...
Investigative Opthalmology & Visual Science.  63 (2022)  4 - p. 20 , 2022
Link: https://doi.org/10.1167/..
 
?
5

Whole genome sequencing for USH2A-associated disease reveal..:

Reurink, Janine ; Weisschuh, Nicole ; Garanto, Alejandro...
https://research.rug.nl/en/publications/33968473-8cf1-49e9-85da-4089312f325a.  , 2023
Link: https://hdl.handle.net/1..
 
?
6

Whole genome sequencing for USH2A-associated disease reveal..:

Reurink, Janine ; Weisschuh, Nicole ; Garanto, Alejandro...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9918427/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
?
7

Whole genome sequencing for USH2A-associated disease reveal..:

Reurink, Janine ; Weisschuh, Nicole ; Garanto, Alejandro...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.xhgg.2023.100181.  , 2023
Link: https://hdl.handle.net/2..
 
?
8

Homozygous Knockout of Cep250 Leads to a Relatively Late-On..:

Abu-Diab, Alaa ; Gopalakrishnan, Prakadeeswari ; Matsevich, Chen...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9987170/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
?
9

ABCA4 c.859-25A>G, a Frequent Palestinian Founder Mutation ..:

Corradi, Zelia ; Salameh, Manar ; Khan, Mubeen...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055564/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
?
10

Resolving the dark matter of ABCA4 for 1054 Stargardt disea..:

Khan, Mubeen ; Cornelis, Stéphanie S ; Del Pozo Valero, Marta...
info:eu-repo/semantics/altIdentifier/doi/.  ,
Link: http://hdl.handle.net/11..
 
?
11

Whole genome sequencing for USH2A-associated disease reveal..:

Janine Reurink ; Nicole Weisschuh ; Alejandro Garanto...
http://www.sciencedirect.com/science/article/pii/S2666247723000131.  , 2023
Link: https://doi.org/10.1016/..
 
1-11