Detalhe da pesquisa
1.
A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl.
Clin Case Rep
; 12(2): e8551, 2024 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-38415192
2.
Does the survival motor neuron copy number variation play a role in the onset and severity of sporadic amyotrophic lateral sclerosis in Malians?
eNeurologicalSci
; 3: 17-20, 2016 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-29430530
3.
Fahr's syndrome with hyperparathyroidism revealed by seizures and proximal weakness.
eNeurologicalSci
; 15: 100192, 2019 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-31080899