Detalles de la búsqueda
1.
The Role of Cluster C19MC in Pre-Eclampsia Development.
Int J Mol Sci
; 23(22)2022 Nov 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-36430313
2.
Expanding the genetic cause of multiple sulfatase deficiency: A novel SUMF1 variant in a patient displaying a severe late infantile form of the disease.
Mol Genet Metab
; 121(3): 252-258, 2017 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-28566233
3.
Novel 14q11.2 microduplication including the CHD8 and SUPT16H genes associated with developmental delay.
Am J Med Genet A
; 170A(5): 1325-9, 2016 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-26834018
4.
Diagnostic potential of microRNAs Mi 517 and Mi 526 as biomarkers in the detection of hypertension and preeclampsia in the first trimester.
Ginekol Pol
; 2023 Apr 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-37042323
5.
A Successful New Case of Twin Pregnancy in a Patient with Swyer Syndrome-An Up-to-Date Review on the Incidence and Outcome of Twin/Multiple Gestations in the Pure 46,XY Gonadal Dysgenesis.
Int J Environ Res Public Health
; 19(9)2022 04 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-35564421
6.
The role of miRNA-210 in pre-eclampsia development.
Ann Med
; 54(1): 1350-1356, 2022 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-35543206
7.
Analysis of Circulating C19MC MicroRNA as an Early Marker of Hypertension and Preeclampsia in Pregnant Patients: A Systematic Review.
J Clin Med
; 11(23)2022 Nov 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-36498625
8.
Three case reports of patients indicating the diversity of molecular and clinical features of 16p11.2 microdeletion anomaly.
BMC Med Genomics
; 14(1): 76, 2021 03 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-33691695
9.
A new family with spastic paraplegia type 51 and novel mutations in AP4E1.
BMC Med Genomics
; 14(1): 131, 2021 05 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-34006278
10.
Novel Mutations Within Collagen Alpha1(I) and Alpha2(I) Ligand-Binding Sites, Broadening the Spectrum of Osteogenesis Imperfecta - Current Insights Into Collagen Type I Lethal Regions.
Front Genet
; 12: 692978, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34306033
11.
Molecular and clinical characterization of new patient with 1,08 Mb deletion in 10p15.3 region.
Mol Cytogenet
; 10: 34, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28912834
12.
Structural and numerical abnormalities resolved in one-step analysis: the most common chromosomal rearrangements detected by comparative genomic hybridization in childhood acute lymphoblastic leukemia.
Cancer Genet Cytogenet
; 200(2): 161-6, 2010 Jul 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-20620600
Resultados
1 -
12
de 12
1
Próxima >
>>