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Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: a case report.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
First application of next-generation sequencing in four families with Wilson disease in Morocco.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s43042-023-00437-7
- By:
- Publication type:
- Article
Early diagnosis of congenital muscular pathologies using next-generation sequencing: experiences from a tertiary center in Morocco.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s43042-023-00416-y
- By:
- Publication type:
- Article
Investigation of bacterial diversity using 16S rRNA sequencing and prediction of its functionalities in Moroccan phosphate mine ecosystem.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-07765-5
- By:
- Publication type:
- Article
Novel copy number variation of COLQ gene in a Moroccan patient with congenital myasthenic syndrome: a case report and review of the literature.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Investigation of bacterial diversity using 16S rRNA sequencing and prediction of its functionalities in Moroccan phosphate mine ecosystem.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-07765-5
- By:
- Publication type:
- Article
Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia.
- Published in:
- Pan African Medical Journal, 2021, v. 39, p. 1, doi. 10.11604/pamj.2021.39.72.27220
- By:
- Publication type:
- Article
Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report.
- Published in:
- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-00959-2
- By:
- Publication type:
- Article