Detalhe da pesquisa
1.
Uncommon runs of homozygosity disclose homozygous missense mutations in two ciliopathy-related genes (SPAG17 and WDR35) in a patient with multiple brain and skeletal anomalies.
Eur J Med Genet;
61(3): 161-167, 2018 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29174089