Table 5.
Genetics studies and literature using PubMed scientific publications Browser (Sefiani et al. 1988; Tajir et al. 2012; Grant et al. 2013; Makrythanasis et al. 2014; Mansouri et al. 2014; Natiq et al. 2014; Qrafli et al. 2014, 2014; Janati Idrissi et al. 2015; Ratbi et al. 2015; Twigg et al. 2016; Elalaoui et al. 2016; Guaoua et al. 2016; Jouali et al. 2016)
| Author | Title | Genetics method | Field | Year |
|---|---|---|---|---|
| Guaoua S et al. | NAT2 Genotypes in Moroccan Patients with Hepatotoxicity Due to Antituberculosis Drugs. | Sanger sequencing and real‐time polymerase chain reaction. | Pharmacogenetics | 2016 |
| Elalaoui SC et al. | Further evidence of POP1 mutations as the cause of anauxetic dysplasia. | Sanger sequencing | Mendelian genetics | 2016 |
| Jouali F et al. | First application of next‐generation sequencing in Moroccan breast/ovarian cancer families and report of a novel frameshift mutation of the BRCA1 gene. | NGS‐targeted sequencing | Cancer genetics | 2016 |
| Twigg SR et al. | Acromelic frontonasal dysostosis and ZSWIM6 mutation: phenotypic spectrum and mosaicism. | NGS and deep sequencing for mosaicism evaluation | Mendelien genetics | 2016 |
| Janati Idrissi M et al. | TPMT alleles in Moroccan. | Allele‐specific PCR and PCR‐RFLP genotyping | Pharmacogenetics | 2015 |
| Ratbi I et al. | Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome‐Biogenesis Genes PEX1 and PEX6. | Exome sequencing | Metabolic genetics | 2015 |
| Mansouri M et al. | A novel nonsense mutation in SCN9A in a Moroccan child with congenital insensitivity to pain. | Sanger sequencing | Mendelian genetics | 2014 |
| Makrythanasis P et al. | Diagnostic exome sequencing to elucidate the genetic basis of likely recessive disorders in consanguineous families. | Exome sequencing with Array CGH | Mendelien genetics | 2014 |
| Natiq A et al. | A new case of de novo 19p13.2p13.12 deletion in a girl with overgrowth and severe developmental delay. | Cytogenetics, molecular cytogenetics, array CGH, Methyl PCR | Clinical Cytogenetics | 2014 |
| Qrafli M et al. | The CYP7A1 gene rs3808607 variant is associated with susceptibility of tuberculosis in Moroccan population. | Real Time PCR and RFLP‐PCR genotyping | Genetic association studies | 2014 |
| Grant AV et al. | Age‐dependent association between pulmonary tuberculosis and common TOX variants in the 8q12‐13 linkage region. | Positional‐cloning approach for linkage‐disequilibrium mapping of an identified susceptibility locus in chromosomal region. | Genetics Linkage analysis | 2013 |
| Tajir M et al. | Pyruvate dehydrogenase deficiency caused by a new mutation of PDHX gene in two Moroccan patients. | Sanger sequencing | Mitochondrial genetics | 2012 |
| Sefiani A et al. | Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11. | X chromosome DNA probes | Genetic linkage analysis | 1988 |