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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 11, 2021
[Experience and lessons on guiding and governing clinical applications of chromosome microarray analysis in the United States]Xiaolei Xie, Jingwei Yu, Zhongxia Qi, et al.
Global Medical Genetics|June 16, 2022
Genotype-Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of LiteratureXiaolei Xie, Hongyan Chai, Autumn DiAdamo, et al.
Molecular Cytogenetics|December 24, 2015
Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literatureQin Wang, Weiqing Wu, Zhiyong Xu, et al.
Materials (Basel, Switzerland)|April 24, 2025
Oily Long-Term Anti-Icing Coating Based on Hydrophobic Cross-Linking Composite ResinZhen Xiao, Mingyang Du, Peining Li, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|July 6, 2015
Changes in and Efficacies of Indications for Invasive Prenatal Diagnosis of Cytogenomic Abnormalities: 13 Years of Experience in a Single CenterJinlai Meng, Chelsea Matarese, Julianna Crivello, et al.
Molecular Cytogenetics|January 14, 2014
Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disabilityFang Xu, Lun Li, Vincent P Schulz, et al.
SSM - Population Health|July 28, 2026
Home-based telework and worker health and well-being across service occupations: A critical interpretive synthesisJuyeon Lee, Yasmeen Almomani, Abbey Davis, et al.
Medical Sciences (Basel, Switzerland)|January 26, 2019
Integrated FISH, Karyotyping and aCGH Analyses for Effective Prenatal Diagnosis of Common Aneuploidies and Other Cytogenomic AbnormalitiesHongyan Chai, Autumn DiAdamo, Brittany Grommisch, et al.
Nano Letters|November 7, 2022
Ultralow-Loss Phonon Polaritons in the Isotope-Enriched α-MoO3Yongqian Zhao, Jiancui Chen, Mengfei Xue, et al.
American Journal of Medical Genetics. Part A|January 7, 2004
FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6Hui Z Zhang, Peining Li, Dongmei Wang, et al.
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