Detalhe da pesquisa
1.
Pure trisomy 2p syndrome in two siblings with an unbalanced translocation and minimal terminal 12q monosomy characterized by high-density microarray.
Cytogenet Genome Res
; 142(4): 249-54, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24751616
2.
Pluripotent Stem Cells as a Model for Human Embryogenesis.
Cells
; 12(8)2023 04 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37190101
3.
Increased proliferation and neuronal fate in prairie vole brain progenitor cells cultured in vitro: effects by social exposure and sexual dimorphism.
Biol Sex Differ
; 14(1): 77, 2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37919790
4.
Association of the EPAS1 rs7557402 Polymorphism with Hemodynamically Significant Patent Ductus Arteriosus Closure Failure in Premature Newborns under Pharmacological Treatment with Ibuprofen.
Diagnostics (Basel)
; 13(15)2023 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37568921
5.
Prenatal prevalence of skeletal dysplasias and a proposal ultrasonographic diagnosis approach.
Rev Invest Clin
; 64(5): 429-36, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23544305
6.
Major craniofacial defects: case series and prenatal diagnosis at the Instituto Nacional de Perinatología, Mexico.
Rev Invest Clin
; 64(5): 420-8, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23544304
7.
El papel de la genética en la restricción del crecimiento intrauterino / The role of genetics in fetal growth restriction
Perinatol. reprod. hum
; 26(2): 35-42, abr.-jun. 2012. ilus, tab
Artigo
em Espanhol
| LILACS | ID: lil-695083