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1. Bi-allelic variants in WDR47 cause a complex neurodevelopmental syndrome

2. Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations

3. Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy

5. Enhancing sustainable healthcare practices through energy-efficient wireless body area networks

9. IEEE 802.15.6 and LoRaWAN for WBAN in Healthcare: A Comparative Study on Communication Efficiency and Energy Optimization

11. Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders

12. Geotechnical correlations of soil properties in Hilla City – Iraq

13. Salam As Banking Financing for Agriculture in Developing Countries: Lessons From Sudan

15. Case report: Clinical and genetic characterization of a novel ALDH7A1 variant causing pyridoxine-dependent epilepsy, developmental delay, and intellectual disability in two siblings.

16. IEEE 802.15.6 and LoRaWAN for WBAN in Healthcare: A Comparative Study on Communication Efficiency and Energy Optimization.

35. Authenticity and quality of muscle foods : assessing consumer trust and fraud detection approaches

36. Effect of Air Pollutants Particulate Matter PM2.5, PM10, Carbon Monoxide (CO), Nitrogen Dioxide (NO2), Sulfur Dioxide (SO2), and Ozone (O3) on Fractional Exhaled Nitric Oxide (FeNO).

37. The morbid genome of ciliopathies: an update

38. Role of nano-capacitor on dielectric constant enhancement in PEO:NH4SCN:xCeO2 polymer nano-composites: Electrical and electrochemical properties

40. Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases

42. Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population

43. Autozygome and high throughput confirmation of disease genes candidacy

44. Genomic and phenotypic delineation of congenital microcephaly

45. Bi-allelic PRRT2variants may predispose to Self-limited Familial Infantile Epilepsy

47. Assessing the Impact of Using (FRP) Material for Strengthening the Holes in (RC) Beams.

49. Bi-allelic variants inWDR47lead to neuronal loss causing a rare neurodevelopmental syndrome with corpus callosum dysgenesis in humans

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