Detalhe da pesquisa
1.
Do research participants share genomic screening results with family members?
J Genet Couns
; 31(2): 447-458, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34665896
2.
Genetic association meta-analysis: a new classification to assess ethnicity using the association of MCP-1 -2518 polymorphism and tuberculosis susceptibility as a model.
BMC Genet
; 16: 128, 2015 Oct 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-26518714
3.
Global health for rare diseases through primary care.
Lancet Glob Health
; 12(7): e1192-e1199, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38876765
4.
A new algorithm DEtectS critical Congenital Heart Disease at different altitudes: ANDES-CHD study.
J Perinatol
; 44(3): 373-378, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38308011
5.
[The SYNTAX Revascularization Index and major cardiovascular events in patients with multivessel coronary artery disease in the Instituto Nacional de Cardiología Ignacio Chávez - Mexico]. / Índice de revascularización SYNTAX y eventos cardiovasculares mayores en pacientes con enfermedad coronaria multiarterial en el Instituto Nacional de Cardiología Ignacio Chávez - México.
Arch Peru Cardiol Cir Cardiovasc
; 4(1): 7-12, 2023.
Artigo
em Espanhol
| MEDLINE | ID: mdl-37583449
6.
[Copy number variation and parental consanguinity elevated in newborns of high altitude with major congenital anomalies in Perú]. / Variantes en el número de copias y consanguinidad parental en neonatos de altura con anomalías congénitas en Perú.
Rev Fac Cien Med Univ Nac Cordoba
; 79(2): 132-140, 2022 06 06.
Artigo
em Espanhol
| MEDLINE | ID: mdl-35700460
7.
Allelic and genotypic frequencies of NAT2, CYP2E1, and AADAC genes in a cohort of Peruvian tuberculosis patients.
Mol Genet Genomic Med
; 9(10): e1764, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34510815
8.
Considering Proximal Urea Cycle Disorders in Expanded Newborn Screening.
Int J Neonatal Screen
; 6(4)2020 Oct 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33124615
9.
Beliefs and Values About Gene Therapy and In-Utero Gene Editing in Patients with Hemophilia and Their Relatives.
Patient
; 13(5): 633-642, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32794073
10.
Variantes en el número de copias en trastornos del neurodesarrollo, síndrome malformativo y talla baja en Perú / Copy number variation in development disorders, malformative syndrome and short stature in Peru
Acta méd. peru
; 37(2): 145-155, abr-jun 2020. tab, graf
Artigo
em Espanhol
|
LILACS-Express
| ID: biblio-1141989
11.
Análisis bibliométrico de la producción científica sobre las agendas nacionales de investigación en el Perú 2011-2014 / Bibliometric analysis of scientific production on research national agenda in Peru 2011-2014
An. Fac. Med. (Perú)
; 77(3): 241-249, 2016. tab
Artigo
em Espanhol
|
LILACS-Express
| ID: biblio-1038211