Detalhe da pesquisa
1.
The prevalence and phenotypic range associated with biallelic PKDCC variants.
Clin Genet
; 104(1): 121-126, 2023 07.
Artigo
Inglês
| MEDLINE | ID: mdl-36896672
2.
Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico.
Front Genet
; 14: 1293929, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-38327701