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1.
An assessment of the analytical performance of non-invasive prenatal testing (NIPT) in detecting sex chromosome aneuploidies: 34,717-patient sample in a single prenatal diagnosis Centre in China.
J Gene Med
; 23(9): e3362, 2021 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-33973298
2.
[Factors affecting the failure of non-invasive prenatal testing and the feasibility analysis of retesting].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(6): 603-608, 2020 Jun 10.
Artículo
en Zh
| MEDLINE | ID: mdl-32472533
3.
Targeted next-generation sequencing identification of mutations in patients with disorders of sex development.
BMC Med Genet
; 17: 23, 2016 Mar 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-26980296
4.
[Prenatal diagnosis of a case with combined Wolf-Hirschhorn syndrome and Jacobsen syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 32(4): 512-4, 2015 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-26252097
5.
[Positive maternal blood cfDNA test caused by confined placental mosaicism in a case].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(6): 627-628, 2020 06 10.
Artículo
en Zh
| MEDLINE | ID: mdl-32472538
6.
A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencing.
Hum Mutat
; 35(5): 625-36, 2014 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-24610732
7.
Xp22.31 copy number variations in 87 fetuses: refined genotype-phenotype correlations by prenatal and postnatal follow-up.
BMC Med Genomics
; 16(1): 69, 2023 04 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-37013593
8.
CpG island methylation status of miRNAs in esophageal squamous cell carcinoma.
Int J Cancer
; 130(7): 1607-13, 2012 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-21547903
9.
Prenatal Diagnosis and Genetic Analysis of 21q21.1-q21.2 Aberrations in Seven Chinese Pedigrees.
Front Genet
; 12: 731815, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34992628
10.
Polymorphisms of decoy receptor 3 are associated with risk of esophageal squamous cell carcinoma in Chinese Han.
Tumour Biol
; 31(5): 443-9, 2010 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-20567955
11.
A functional variation in pre-microRNA-196a is associated with susceptibility of esophageal squamous cell carcinoma risk in Chinese Han.
Biomarkers
; 15(7): 614-8, 2010 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-20722507
12.
Prenatal diagnosis of familial submicroscopic duplication at 18q22.3 without phenotypic abnormalities.
Taiwan J Obstet Gynecol
; 59(3): 446-450, 2020 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-32416897
13.
A retrospective analysis the clinic data and follow-up of non-invasive prenatal test in detection of fetal chromosomal aneuploidy in more than 40,000 cases in a single prenatal diagnosis center.
Eur J Med Genet
; 63(9): 104001, 2020 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-32622960
14.
Detection of fetal trisomy and single gene disease by massively parallel sequencing of extracellular vesicle DNA in maternal plasma: a proof-of-concept validation.
BMC Med Genomics
; 12(1): 151, 2019 11 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-31684971
15.
Genome-wide detection of additional fetal chromosomal abnormalities by cell-free DNA testing of 15,626 consecutive pregnant women.
Sci China Life Sci
; 62(2): 215-224, 2019 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-30076564
16.
A functional varient in microRNA-146a is associated with risk of esophageal squamous cell carcinoma in Chinese Han.
Fam Cancer
; 9(4): 599-603, 2010 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-20680470
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