Detalles de la búsqueda
1.
Association of TP53 rs1042522 G > C, MDM2 rs2279744 T > G, and miR-34b/c rs4938723 T > C polymorphisms with aneuploidy pregnancy susceptibility.
BMC Pregnancy Childbirth
; 23(1): 624, 2023 Aug 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-37648962
2.
Ultrasonographic classification of 26 cases of fetal umbilical-portal-systemic venous shunts and the correlations with fetal chromosomal abnormalities.
BMC Pregnancy Childbirth
; 23(1): 236, 2023 Apr 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-37038108
3.
The relationship of maternal polymorphisms of genes related to meiosis and DNA damage repair with fetal chromosomal stability.
J Perinat Med
; 51(8): 1082-1096, 2023 Oct 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-37486214
4.
Identification of a Novel 7-bp Deletion in the α-Globin Gene Cluster in One Chinese Family.
Hemoglobin
; 47(2): 49-51, 2023 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-37247201
5.
Factors associated with fetal karyotype in spontaneous abortion: a case-case study.
BMC Pregnancy Childbirth
; 22(1): 320, 2022 Apr 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-35421926
6.
Gene mutations in children with permanent congenital hypothyroidism in Yunnan, China.
Zhejiang Da Xue Xue Bao Yi Xue Ban
; 51(3): 306-313, 2022 Jun 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-36207832
7.
Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis.
BMC Pregnancy Childbirth
; 21(1): 496, 2021 Jul 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-34238233
8.
First-trimester maternal serum alpha-fetoprotein is not a good predictor for adverse pregnancy outcomes: a retrospective study of 3325 cases.
BMC Pregnancy Childbirth
; 20(1): 104, 2020 Feb 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-32050927
9.
[Result of carrier screening for spinal muscular atrophy among 3049 reproductive-age individuals from Yunnan region].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(4): 384-388, 2020 Apr 10.
Artículo
en Zh
| MEDLINE | ID: mdl-32219818
10.
LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathies.
Hum Mutat
; 40(12): 2221-2229, 2019 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-31286593
11.
Evaluation of portable colposcopy and human papillomavirus testing for screening of cervical cancer in rural China.
Int J Gynecol Cancer
; 29(1): 23-27, 2019 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30640679
12.
A rat model of placental inflammation explains the unexplained elevated maternal serum alpha-fetoprotein associated with adverse pregnancy outcomes.
J Obstet Gynaecol Res
; 45(10): 1980-1988, 2019 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-31381236
13.
[Association of copy number of SMN1 and SMN2 with clinical phenotypes in children with spinal muscular atrophy].
Zhongguo Dang Dai Er Ke Za Zhi
; 21(3): 239-243, 2019 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-30907347
14.
[Discussion on the standard of clinical genetic testing report and the consensus of gene testing industry].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(1): 1-8, 2018 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-29419850
15.
Next-generation sequencing improves thalassemia carrier screening among premarital adults in a high prevalence population: the Dai nationality, China.
Genet Med
; 19(9): 1022-1031, 2017 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-28125089
16.
[Advance in clinical application of non-invasive prenatal screening using cell-free fetal DNA].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 34(6): 924-927, 2017 Dec 10.
Artículo
en Zh
| MEDLINE | ID: mdl-29188632
17.
[Genetic analysis and prenatal diagnosis for a pregnant woman with an unbalanced t(1;2), t(6;7) translocation and intellectual disability].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 34(4): 583-587, 2017 Aug 10.
Artículo
en Zh
| MEDLINE | ID: mdl-28777864
18.
[Analysis of treatment efficacy for congenital hypothyroidism in some regions of Yunnan Province, China].
Zhongguo Dang Dai Er Ke Za Zhi
; 19(7): 741-747, 2017 Jul.
Artículo
en Zh
| MEDLINE | ID: mdl-28697824
19.
[Application of BoBs technique for detecting common chromosome microdeletion and microduplication syndromes].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 33(4): 452-7, 2016 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-27454996
20.
[Mutations of phenylalanine hydroxylase gene detected in 20 patients with phenylketonuria from Yunnan Province].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 32(2): 153-7, 2015 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-25863075