12 results on '"Adadi, Najlae"'
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2. Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
3. High frequency of hotspot mutation in PTPN11 gene among Moroccan patients with Noonan syndrome
4. Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly
5. Post-mortem diagnosis of Pompe disease by exome sequencing in a Moroccan family: a case report
6. Correlation genotype-phenotype: MEFV gene mutations and Moroccan patients with rheumatoid arthritis
7. Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot (Genetics in Medicine, (2021), 23, 10, (1952-1960), 10.1038/s41436-021-01212-y)
8. High frequency of hotspotmutation in PTPN11gene among Moroccan patients with Noonan syndrome
9. First application of next-generation sequencing in patients with hypertrophic cardiomyopathy in Morocco and report of a novel frameshift mutation of MYBPC3 gene: Case report
10. Inherited dilated cardiomyopathy in a large Moroccan family caused by LMNA mutation
11. Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death
12. Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.
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