Detalhe da pesquisa
1.
22q11.2 Deletion Syndrome in Colombian Patients With Syndromic Cleft Lip and/or Palate.
Cleft Palate Craniofac J
; 56(1): 116-122, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29652534
2.
CNVs in the 22q11.2 Chromosomal Region Should Be an Early Suspect in Infants with Congenital Cardiac Disease.
Clin Med Insights Cardiol
; 15: 11795468211016870, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34104029
3.
Disorders of sex development: Genetic characterization of a patient cohort.
Mol Med Rep
; 21(1): 97-106, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31746433
4.
Caracterización fenotípica de pacientes sometidos a autopsia perinatal en el Hospital Universitario San Ignacio / Phenotypical Characterization of Patients Submitted to Perinatal Autopsy at the Hospital Universitario San Ignacio
Univ. med
; 60(1)2019.
Artigo
em Espanhol
| LILACS, COLNAL | ID: biblio-995049