Namik Kaya and Hospital And Research - Free people check

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Mutations in C2orf37, Encoding a Nucleolar Protein, Cause ...

www.cell.com

by AM Alazami · · Cited by 130 — Namik Kaya. Namik Kaya. Affiliations. Department of Genetics, King Faisal Spe…t Hospital and Research Center, Riyadh , ... › fulltext

ISCA2 mutation causes infantile neurodegenerative mitochondrial...

jmg.bmj.com

Namik Kaya 3, 6; 1 Department of Medical Genetics, King Faisal Spe…t Hospital and Research Center, Riyadh, Saudi Arabia 2 College of Medicine, Alfaisal ...

KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital...

jmg.bmj.com

…spondence to Dr Namik Kaya, Department of Genetics, King Faisal Spe…t Hospital and Research Centre, MBC:03, P.O. Box 3354, ...

Prevalence of PIK3CA mutations and the SNP rs in ...

www.tandfonline.com

by B Karakas · · Cited by 29 — Namik Kaya Department of Genetics; King Faisal Spe…t Hospital and Research Center; Riyadh, Saudi Arabia. ,. Hazem Ghebeh Department of Stem Cell ... › ... › Volume 14, Issue 10

Acta Neuropathologica - KAUST Repository

repository.kaust.edu.sa

by M AlMuhaizea · · Cited by 15 — Namik Kaya, PhD. King Faisal Spe…t Hospital and Research Center. Riyadh, - SAUDI ARABIA. …sponding Author Secondary. Information:. › bitstream › ANEU...

The clinical utility of molecular karyotyping for neurocognitive ...

www.gimjournal.org

by SM Al-Qattan · · Cited by 18 — Namik Kaya, PhD. Namik Kaya. Affiliations. Department of Genetics, Research Center, King Faisal Spe…t Hospital and Research Center, Riyadh, ... › article › abstract

Truncating mutations in YIF1B cause a progressive ...

repub.eur.nl

by M AlMuhaizea · · Cited by 15 — Ε Namik Kaya .sa. 1. Department of Neurosciences, King Faisal Spe…t. Hospital and Research Centre (KFSHRC), Riyadh,. Saudi Arabia. › pub › Repub

Chromosome 12q q deletion causes multiple dysmorphic...

molecularcytogenetics.biomedcentral.com

... Namik Kaya .sa. Author Affiliations. 1 Department of Genetics, King Faisal Spe…t Hospital and Research Centre, Riyadh,

Phenotypic Variability of MEGF10 Variants Causing MDPI

www.mdpi.com

by M AlMuhaizea · — Namik Kaya. 2,*. 1. Neuroscience Center, King Faisal Spe…t Hospital and Research Center, Riyadh , Saudi Arabia. › ...

All web results to the name "Namik Kaya"

Home - Human Disease Genes

humandiseasegenes.nl

Nov 3, — Dr. Namik Kaya, PhD (Senior Scientist, Head, Cognitive Genetics Unit), Department of Genetics, King Faisal Spe…t Hospital and Research ... › kcna4

Namik Kaya - اقتباسات الباحث العلمي من Google

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Namik Kaya. King Faisal Spe…t Hospital and Research Center. Molecular Genetics, Medical Genomics, NeuroGenetics, Molecular Cytogenetics/Pathology, ...

Integrated Left Ventricular Global Transcriptome and Proteome...

journals.plos.org

Namik Kaya,. Affiliation Genetics Department, King Faisal Spe…t Hospital and Research Centre, RiyadhSaudi Arabia. ⨯. Nzioka P.

"Comparison of Two Dependent within Subject Coefficients of Variation...

ir.lib.uwo.ca

Namik Kaya, King Faisal Spe…t Hospital and Research Centre, Saudi Arabia Allan Donner, University of Western Ontario. Document Type. Article. Publication Date.

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