Detalhe da pesquisa
1.
Different effects of maternal homocysteine concentration, MTHFR and MTRR genetic polymorphisms on the occurrence of fetal aneuploidy.
Reprod Biomed Online
; 45(6): 1207-1215, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36210274
2.
Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome.
J Biomed Sci
; 23(1): 48, 2016 Jun 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27266699
3.
Prevalence of human papillomavirus infection in esophageal and cervical cancers in the high incidence area for the two diseases from 2007 to 2009 in Linzhou of Henan Province, Northern China.
Arch Virol
; 159(6): 1393-401, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24385156
4.
Polymorphic distribution and forensic effectiveness study of eight miniSTR in Chinese Uyghur ethnic group.
Mol Biol Rep
; 41(4): 2371-5, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24469714
5.
[Detection and prenatal diagnosis for RS1 gene mutations in two Chinese families with X-linked juvenile retinoschisis].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 30(2): 199-202, 2013 Apr.
Artigo
em Zh
| MEDLINE | ID: mdl-23568735
6.
[Analysis of CYP17A1 gene mutation in a child patient with 17 alpha-hydroxylase/17, 20-lyase deficiency].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 30(4): 439-42, 2013 Aug.
Artigo
em Zh
| MEDLINE | ID: mdl-23926012
7.
[Efficiency of multiplex ligation-dependent probe amplification combined with short tandem repeat linkage analysis for the prenatal diagnosis for Duchenne muscular dystrophy].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 30(1): 40-4, 2013 Feb.
Artigo
em Zh
| MEDLINE | ID: mdl-23450477
8.
[Maternal cell contamination of prenatal samples and the potential effects on prenatal diagnosis results].
Zhonghua Fu Chan Ke Za Zhi
; 48(2): 86-91, 2013 Feb.
Artigo
em Zh
| MEDLINE | ID: mdl-23544487
9.
[Significance of detecting free DNA from maternal plasma for the diagnosis of fetal chromosomal aneuploidies].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 29(4): 435-8, 2012 Aug.
Artigo
em Zh
| MEDLINE | ID: mdl-22875501
10.
[Association of methionine synthase reductase gene polymorphism with unexplained recurrent spontaneous abortion].
Zhonghua Fu Chan Ke Za Zhi
; 47(10): 742-6, 2012 Oct.
Artigo
em Zh
| MEDLINE | ID: mdl-23302731
11.
[Clinical application of noninvasive prenatal diagnosis using cell free fetal DNA in maternal plasma].
Zhonghua Fu Chan Ke Za Zhi
; 47(11): 813-7, 2012 Nov.
Artigo
em Zh
| MEDLINE | ID: mdl-23302120
12.
Nicotine Ingestion Reduces Heart Rate Variability in Young Healthy Adults.
Biomed Res Int
; 2022: 4286621, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35028314
13.
Rapid screening for chromosomal aneuploidies using array-MLPA.
BMC Med Genet
; 12: 68, 2011 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-21575262
14.
Parental Genetic Variants, MTHFR 677C>T and MTRR 66A>G, Associated Differently with Fetal Congenital Heart Defect.
Biomed Res Int
; 2017: 3043476, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28758112
15.
Detection of fetal epigenetic biomarkers through genome-wide DNA methylation study for non-invasive prenatal diagnosis.
Mol Med Rep
; 15(6): 3989-3998, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28440505
16.
Prenatal diagnosis for a Chinese family with a de novo DMD gene mutation: A case report.
Medicine (Baltimore)
; 96(50): e8814, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29390271
17.
Clinical findings and molecular cytogenetic study of de novo pure chromosome 9p deletion: Pre- and postnatal diagnosis.
Taiwan J Obstet Gynecol
; 55(6): 867-870, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28040136
18.
Analysis of etiology, chromosome and prognosis for small left heart system development in 69 fetuses.
J Matern Fetal Neonatal Med
; 29(3): 493-503, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-25731651
19.
[Screening for chromosomal abnormalities using nuchal translucency measurement with materal serum biochemistry markers in first trimester].
Beijing Da Xue Xue Bao Yi Xue Ban
; 37(1): 39-41, 2005 Feb 18.
Artigo
em Zh
| MEDLINE | ID: mdl-15719038
20.
[Establishment of permanent lymphoblastoid cell lines of 47 patients with abnormal chromosome karyotype].
Yi Chuan Xue Bao
; 29(4): 303-6, 2002 Apr.
Artigo
em Japonês
| MEDLINE | ID: mdl-11985262