Detalles de la búsqueda
1.
[Analysis and clinical application of preimplantation genetic testing for monogenic disorders in a case with Spinal muscular atrophy "2+0" genotype].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 41(3): 294-299, 2024 Mar 10.
Artículo
en Zh
| MEDLINE | ID: mdl-38448017
2.
Effect of noninvasive embryo viability testing versus conventional IVF on the live birth rate in IVF/ICSI patients: a study protocol for a double-blind, multicenter, randomized controlled trial.
BMC Pregnancy Childbirth
; 23(1): 641, 2023 Sep 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-37674133
3.
A novel multifunctional haplotyping-based preimplantation genetic testing for different genetic conditions.
Hum Reprod
; 37(11): 2546-2559, 2022 10 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-36066440
4.
Individual-based morphological brain network organization and its association with autistic symptoms in young children with autism spectrum disorder.
Hum Brain Mapp
; 42(10): 3282-3294, 2021 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-33934442
5.
[Data analysis of non-invasive prenatal testing based on special loci in cell-free fetal DNA].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(1): 56-59, 2018 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-29419861
6.
Next generation sequencing as a new detection strategy for maternal cell contamination in clinical prenatal samples.
Ginekol Pol
; 89(6): 326-334, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-30010182
7.
Identification and interruption of inheritance of familial cryptic translocations: A case report.
Mol Genet Genomic Med
; 12(1): e2356, 2024 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-38284442
8.
Preimplantation genetic testing as a means of preventing hereditary congenital myasthenic syndrome caused by RAPSN.
Mol Genet Genomic Med
; 12(3): e2409, 2024 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-38511267
9.
The infertile individual analysis based on whole-exome sequencing in chinese multi-ethnic groups.
Genes Genomics
; 45(4): 531-542, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-36115009
10.
F8 gene inversion and duplication cause no obvious hemophilia A phenotype.
Front Genet
; 14: 1098795, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-36845383
11.
Rapid and non-invasive diagnostic techniques for embryonic developmental potential: a metabolomic analysis based on Raman spectroscopy to identify the pregnancy outcomes of IVF-ET.
Front Cell Dev Biol
; 11: 1164757, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37427383
12.
Dynamic peripheral blood microRNA expression landscape during the peri-implantation stage in women with successful pregnancy achieved by single frozen-thawed blastocyst transfer.
Hum Reprod Open
; 2023(4): hoad034, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37700872
13.
Case Report: A Paternal 20q13.2-q13.32 Deletion Patient With Growth Retardation Improved by Growth Hormone.
Front Genet
; 13: 859185, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35401665
14.
Non-invasive Metabolomic Profiling of Embryo Culture Medium Using Raman Spectroscopy With Deep Learning Model Predicts the Blastocyst Development Potential of Embryos.
Front Physiol
; 12: 777259, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34867485
15.
NEURO-LEARN: a Solution for Collaborative Pattern Analysis of Neuroimaging Data.
Neuroinformatics
; 19(1): 79-91, 2021 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32524429
16.
Application of single-sperm sequencing in a male with Marfan syndrome: a case report and a literature review.
J Genet
; 1002021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34057151
17.
Effects of Brain Atlases and Machine Learning Methods on the Discrimination of Schizophrenia Patients: A Multimodal MRI Study.
Front Neurosci
; 15: 697168, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34385901
18.
The gut microbiome is associated with brain structure and function in schizophrenia.
Sci Rep
; 11(1): 9743, 2021 05 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-33963227
19.
Divergent Alterations of Structural-Functional Connectivity Couplings in First-episode and Chronic Schizophrenia Patients.
Neuroscience
; 460: 1-12, 2021 04 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-33588002
20.
Haplotyping by linked-read sequencing (HLRS) of the genetic disease carriers for preimplantation genetic testing without a proband or relatives.
BMC Med Genomics
; 13(1): 117, 2020 08 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-32819358