Detalhe da pesquisa
1.
The influence of six polymorphisms of uncoupling protein 3 (UCP3) gene and childhood obesity: a case-control study.
BMC Pediatr
; 23(1): 87, 2023 02 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36810017
2.
Applicability of gene expression profile of childhood acute lymphoblastic leukemia at diagnosis and at the end of the induction phase of chemotherapy at a cancer hospital in the state of Goiás (Brazil).
Tumour Biol
; 35(2): 1397-402, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24052438
3.
c.1103T>C (p.Ile368Th) de novo Variant in Synaptotagmin 1 (SYT1) Gene is Pathogenic, Leading to an Ultra-Rare Neurodevelopmental Disorder: The Baker-Gordon Syndrome.
Int Med Case Rep J
; 17: 63-70, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38283597
4.
Genomic variations in patients with myelodysplastic syndrome and karyotypes without numerical or structural changes.
Sci Rep
; 11(1): 2783, 2021 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33531543
5.
Comparative proteomical and metalloproteomical analyses of human plasma from patients with laryngeal cancer.
Cancer Immunol Immunother
; 59(1): 173-81, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19629479
6.
Copy Number Gain at Xq28 in a Child with Global Developmental Delay Associated with a Variant Form of Hoyeraal-Hreidarsson Syndrome.
Mol Syndromol
; 10(4): 214-218, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-31602194
7.
Molecular Characterization of Koolen De Vries Syndrome in Two Girls with Idiopathic Intellectual Disability from Central Brazil.
Mol Syndromol
; 8(3): 155-160, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28588437
8.
Challenges in clinical and laboratory diagnosis of androgen insensitivity syndrome: a case report.
J Med Case Rep
; 5: 446, 2011 Sep 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-21902827
9.
An easy procedure for cytogenetic analysis of aged chromosome preparations using FISH-WCP probes.
Chromosome Res
; 10(3): 233-8, 2002.
Artigo
em Inglês
| MEDLINE | ID: mdl-12067212