E-LIB Suche - Ergebnisse für: Al-Raqad, Mohammed

1

Haploinsufficiency of PRR12 causes a spectrum of neurodevel..:

Chowdhury, Fuad ; Wang, Lei ; Al-Raqad, Mohammed...
Genetics in Medicine. 23 (2021) 7 - p. 1234-1245 , 2021

Link: https://doi.org/10.1038/..

2

A homozygous loss-of-function CAMK2A mutation causes growth..:

Chia, Poh Hui ; Zhong, Franklin Lei ; Niwa, Shinsuke...
eLife. 7 (2018) - p. , 2018

Link: https://doi.org/10.7554/..

3

SYT1-associated neurodevelopmental disorder: a case series:

Baker, Kate ; Gordon, Sarah L ; Melland, Holly...
Brain. 141 (2018) 9 - p. 2576-2591 , 2018

Link: https://doi.org/10.1093/..

4

Loss of the scavenger mRNA decapping enzyme DCPS causes syn..:

Ng, Calista K.L. ; Shboul, Mohammad ; Taverniti, Valerio...
Human Molecular Genetics. 24 (2015) 11 - p. 3163-3171 , 2015

Link: https://doi.org/10.1093/..

5

Electrocardiographic Changes in Jordanian Patients With Bec..:

Al-Raqad, Mohammed K ; Alwahsh, Shorouk ; Hejazi, Issa S...
Cureus. , 2023

Link: https://doi.org/10.7759/..

6

Haploinsufficiency of PRR12 causes a spectrum of neurodevel..:

Chowdhury, Fuad ; Wang, Lei ; Al-Raqad, Mohammed...
https://research.rug.nl/en/publications/8b645f00-a2db-4806-8c67-fe341888ac0d. , 2021

Link: https://hdl.handle.net/1..

7

Genome-wide CRISPR-Cas9 screen identifies leukemia-specific..:

Yamauchi, Takuji ; Masuda, Takeshi ; Canver, Matthew C...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849534/. , 2018

Link: http://www.ncbi.nlm.nih...

8

SYT1-associated neurodevelopmental disorder: a case series:

Baker, Kate ; Gordon, Sarah L ; Melland, Holly...
https://www.repository.cam.ac.uk/handle/1810/285739. , 2018

Link: https://www.repository.c..

9

Loss of the scavenger mRNA decapping enzyme DCPS causes syn..:

Ng, Calista K.L ; Shboul, Mohammad ; Taverniti, Valerio...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424953/. , 2015

Link: http://www.ncbi.nlm.nih...

10

SYT1-associated neurodevelopmental disorder: a case series:

Baker, K. (Kate) ; Gordon, S.L. (Sarah L.) ; Melland, H. (Holly)...
http://repub.eur.nl/pub/113427. , 2018

Link: http://repub.eur.nl/pub/..

11

A homozygous loss-of-function CAMK2A mutation causes growth..:

Poh Hui Chia ; Franklin Lei Zhong ; Shinsuke Niwa...
https://elifesciences.org/articles/32451. , 2018

Link: https://doi.org/10.7554/..

12

Organizational Justice and Its Impact on Organizational Com..:

Zamanan, Mohammad S. A. ; Al-Qa'eed, Marzouq Ayed ; Al-Raqad, Mohammad Abed Al-Kareem
Modern Applied Science. 14 (2020) 6 - p. 38 , 2020

Link: https://doi.org/10.5539/..

13

Cyclopia: A Rare Condition with Unusual Presentation - A Ca..:

Salama, Ghassan S.A. ; Kaabneh, Mahmoud A.F. ; Al-Raqad, Mohamed K....
Clinical Medicine Insights: Pediatrics. 9 (2015) - p. CMPed.S21107 , 2015

Link: https://doi.org/10.4137/..

14

G.P.12.07 Cardiac involvement in manifesting female carrier..:

Al-raqad, M.K. ; Aboumousa, A. ; Guglieri, M...
Neuromuscular Disorders. 18 (2008) 9-10 - p. 805-806 , 2008

Link: https://doi.org/10.1016/..

15

Development of Chitosan/Whey Protein Hydrolysate Composite ..:

Al-Hilifi, Sawsan A. ; Al-Ibresam, Orass T. ; Al-Hatim, Raqad R....
Journal of Composites Science. 7 (2023) 3 - p. 94 , 2023

Link: https://doi.org/10.3390/..