Pynaker C, McCoy J, Halliday J, Lewis S, Amor D, Walker S
BMC Pediatr. 2024; 24(1):536.
PMID: 39174956
PMC: 11340052.
DOI: 10.1186/s12887-024-05012-6.
Xu Z, Liu N, Gao L, Yu D
Appl Clin Genet. 2024; 17:85-93.
PMID: 38835973
PMC: 11149622.
DOI: 10.2147/TACG.S461674.
Song T, Xu Y, Li Y, Zheng J, Guo F, Jin X
Reprod Sci. 2023; 31(4):1089-1107.
PMID: 38012523
DOI: 10.1007/s43032-023-01399-2.
Que Y, Cai M, Yang F, Ji Q, Zhang S, Huang W
BMC Pregnancy Childbirth. 2023; 23(1):679.
PMID: 37726736
PMC: 10510157.
DOI: 10.1186/s12884-023-05999-3.
Cai M, Que Y, Chen M, Zhang M, Huang H, Xu L
J Cell Mol Med. 2023; 27(16):2354-2361.
PMID: 37401003
PMC: 10424293.
DOI: 10.1111/jcmm.17821.
Classifying and evaluating fetuses with multicystic dysplastic kidney in etiologic studies.
Cai M, Guo C, Wang X, Lin M, Xu S, Huang H
Exp Biol Med (Maywood). 2023; 248(10):858-865.
PMID: 37208928
PMC: 10484196.
DOI: 10.1177/15353702231164933.
Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndrome.
Cai M, Lin M, Guo N, Fu M, Xu L, Lin N
Front Pediatr. 2022; 10:910497.
PMID: 36034547
PMC: 9399630.
DOI: 10.3389/fped.2022.910497.
Positive predictive value of noninvasive prenatal testing for sex chromosome abnormalities.
Guo N, Cai M, Lin M, Xue H, Huang H, Xu L
Mol Biol Rep. 2022; 49(10):9251-9256.
PMID: 35960415
PMC: 9515017.
DOI: 10.1007/s11033-022-07754-x.
Chromosomal Microarray Analysis in Fetuses Detected with Isolated Cardiovascular Malformation: A Multicenter Study, Systematic Review of the Literature and Meta-Analysis.
Mastromoro G, Khaleghi Hashemian N, Guadagnolo D, Giuffrida M, Torres B, Bernardini L
Diagnostics (Basel). 2022; 12(6).
PMID: 35741137
PMC: 9221891.
DOI: 10.3390/diagnostics12061328.
Single nucleotide polymorphism array in genetic evaluation of fetal ultrasound abnormalities: a retrospective follow-up study.
Huang H, Cai M, Xue H, Xu L, Lin N
Am J Transl Res. 2022; 14(5):3516-3524.
PMID: 35702125
PMC: 9185077.
Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center.
Cai M, Lin N, Su L, Wu X, Xie X, Xu S
J Transl Med. 2022; 20(1):168.
PMID: 35397568
PMC: 8994287.
DOI: 10.1186/s12967-022-03373-z.
Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges-Systematic Review of the Literature and Meta-Analysis.
Mastromoro G, Guadagnolo D, Khaleghi Hashemian N, Marchionni E, Traversa A, Pizzuti A
Diagnostics (Basel). 2022; 12(3).
PMID: 35328129
PMC: 8947110.
DOI: 10.3390/diagnostics12030575.
Prenatal Diagnosis of 17p11.2 Copy Number Abnormalities Associated With Smith-Magenis and Potocki-Lupski Syndromes in Fetuses.
Cai M, Fu X, Xu L, Lin N, Huang H
Front Genet. 2022; 12:779237.
PMID: 34992630
PMC: 8724517.
DOI: 10.3389/fgene.2021.779237.
Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical Outcomes.
Cai M, Huang H, Su L, Wu X, Xie X, Xu L
Risk Manag Healthc Policy. 2021; 14:2491-2497.
PMID: 34163268
PMC: 8214565.
DOI: 10.2147/RMHP.S312813.
Comparative clinical genetic testing in spontaneous miscarriage: Insights from a study in Southern Chinese women.
Cai M, Lin N, Xu L, Huang H
J Cell Mol Med. 2021; 25(12):5721-5728.
PMID: 33973351
PMC: 8184667.
DOI: 10.1111/jcmm.16588.
Variance-Preserving Estimation of Intensity Values Obtained From Omics Experiments.
Ribeiro A, Maria Pavan Soler J, Hirata Jr R
Front Genet. 2019; 10:855.
PMID: 31616468
PMC: 6764481.
DOI: 10.3389/fgene.2019.00855.
Submicroscopic chromosomal imbalances contribute to early abortion.
Li H, Liu M, Xie M, Zhang Q, Xiang J, Duan C
Mol Cytogenet. 2018; 11:41.
PMID: 30038665
PMC: 6054741.
DOI: 10.1186/s13039-018-0386-0.
[Advances on prenatal diagnosis of birth defects associated with genetic disorders].
Yan K, Jin F
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017; 46(3):227-232.
PMID: 29039162
PMC: 10396938.
DOI: 10.3785/j.issn.1008-9292.2017.06.01.
Rawcopy: Improved copy number analysis with Affymetrix arrays.
Mayrhofer M, Viklund B, Isaksson A
Sci Rep. 2016; 6:36158.
PMID: 27796336
PMC: 5086940.
DOI: 10.1038/srep36158.
Association between chromosomal aberration of COX8C and tethered spinal cord syndrome: array-based comparative genomic hybridization analysis.
Zhao Q, Bai S, Cheng C, Tao B, Wang L, Liang S
Neural Regen Res. 2016; 11(8):1333-8.
PMID: 27651783
PMC: 5020834.
DOI: 10.4103/1673-5374.189200.
