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1.
APA scoring system: a novel predictive model based on risk factors of pregnancy loss for recurrent spontaneous abortion patients.
J Obstet Gynaecol;
42(6): 2069-2074, 2022 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-35048758
2.
[Prenatal diagnosis of five fetuses with 7q11.23 microdeletion or microduplication].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi;
38(11): 1064-1067, 2021 Nov 10.
Artículo
en Zh
| MEDLINE | ID: mdl-34729744
3.
[Study on clinical features and diagnostic methods of prenatal Wolf-Hirschhorn syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi;
38(8): 735-739, 2021 Aug 10.
Artículo
en Zh
| MEDLINE | ID: mdl-34365613
4.
[Effectiveness of non-invasive prenatal screening for the detection of fetal sex chromosome anomalies].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi;
38(4): 325-328, 2021 Apr 10.
Artículo
en Zh
| MEDLINE | ID: mdl-33834457
5.
[Impact of confined placental mosaicism on non-invasive prenatal testing and pregnancy outcomes].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi;
38(4): 335-338, 2021 Apr 10.
Artículo
en Zh
| MEDLINE | ID: mdl-33834459
6.
Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age.
J Clin Lab Anal;
34(4): e23117, 2020 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-31762079
7.
[Prenatal diagnosis and clinical analysis of two fetuses with Cat-eye syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi;
36(5): 498-501, 2019 May 10.
Artículo
en Zh
| MEDLINE | ID: mdl-31030443
8.
Application of the BACs-on-Beads™ assay for rapid prenatal detection application of BoBs™ for PND of aneuploidies and microdeletions.
Mol Reprod Dev;
85(2): 146-154, 2018 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-29247566
9.
[Prenatal diagnosis of a fetus with Miller-Dieker syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi;
34(6): 879-883, 2017 Dec 10.
Artículo
en Zh
| MEDLINE | ID: mdl-29188621
10.
Molecular spectrum of ß-thalassemia in Fujian Province, Southeastern China.
Hemoglobin;
37(4): 343-50, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23682686
11.
Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy.
Front Neurosci;
17: 1165601, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37250406
12.
Molecular characterization of a novel 27.6-kb deletion causing α(+) thalassemia in a Chinese family.
Ann Hematol;
90(1): 17-22, 2011 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-20645100
13.
Comprehensive Assessment of Fetal Bilateral Ventriculomegaly Based on Genetic Disorders, Cytomegalovirus Infection, Extra Prenatal Imaging and Pregnancy Outcomes in a Tertiary Referral Center.
Int J Gen Med;
14: 7719-7728, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34764685
14.
Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center.
Mol Cytogenet;
14(1): 56, 2021 Dec 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-34863241
15.
Diagnostic accuracy and value of chromosomal microarray analysis for chromosomal abnormalities in prenatal detection: A prospective clinical study.
Medicine (Baltimore);
100(20): e25999, 2021 May 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-34011095
16.
A new ß-thalassemia deletion mutation [codon 36 (-C)] observed in a Chinese woman.
Hemoglobin;
34(6): 599-603, 2010.
Artículo
en Inglés
| MEDLINE | ID: mdl-21077770
17.
Single nucleotide polymorphism array analysis of 102 patients with developmental delay and/or intellectual disability from Fujian, China.
Clin Chim Acta;
510: 638-643, 2020 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-32858057
18.
LZAP promotes the proliferation and invasiveness of cervical carcinoma cells by targeting AKT and EMT.
J Cancer;
11(6): 1625-1633, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32047568
19.
Long-Molecule Sequencing: A New Approach for Identification of Clinically Significant DNA Variants in α-Thalassemia and ß-Thalassemia Carriers.
J Mol Diagn;
22(8): 1087-1095, 2020 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-32473995
20.
Identification of a novel pre-terminating mutation in human HBB gene as a cause of ß0-thalassemia phenotype.
Int J Clin Exp Pathol;
12(8): 3070-3076, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31934147