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Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Application of next generation sequencing in genetic counseling a case of a couple at risk of cystinosis.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01167-y
- By:
- Publication type:
- Article
A novel frameshift mutation in the XPC gene in a Moroccan patient: a case report.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Clinical description and mutational profile of a Moroccan series of patients with Rubinstein Taybi syndrome.
- Published in:
- African Health Sciences, 2021, v. 21, n. 2, p. 960, doi. 10.4314/ahs.v21i2.58
- By:
- Publication type:
- Article
Familial X/Y Translocation Encompassing ARSE in Two Moroccan Siblings with Sensorineural Deafness.
- Published in:
- 2018
- By:
- Publication type:
- Case Study