Yuan-yuan Zhang

发表

Leukemias, Lymphomas, and Other Related Disorders

J. Rowley, Yuan-yuan Zhang, 2013 .

Molecular and phenotypic characteristics of 15q24 microdeletion in pediatric patients with developmental disorders

Bijun Zhang, Yanyan Zhao, Yuan-yuan Zhang, 2021, Molecular Cytogenetics.

Upregulation of human with-no-lysine kinase-4 gene expression by GATA-1 acetylation.

Yanyan Zhao, Miao Li, Yuan-yuan Zhang, 2009, The international journal of biochemistry & cell biology.

A new mutation in the gene ROR2 causes brachydactyly type B1.

Yuan-yuan Zhang, Dan-Qin Huang, Xiaoliang Liu, 2014, Gene.

Copy number variations of chromosome 17p11.2 region in children with development delay and in fetuses with abnormal imaging ndings

Yuan-yuan Zhang, Shengjing, 2021 .

Copy number variations of chromosome 17p11.2 region in children with development delay and in fetuses with abnormal imaging findings

Guoming Chu, Yanyan Zhao, Yuan-yuan Zhang, 2021, BMC medical genomics.

Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome

Lu Zhang, Bijun Zhang, Yanyan Zhao, 2022, Italian Journal of Pediatrics.

Differences in IGF axis‐related proteins in amniotic fluid of trisomy 21 and trisomy 18 using a multiple reaction monitoring approach

Guangrui Lai, Bijun Zhang, Yanyan Zhao, 2014, Prenatal diagnosis.

Identifying of 22q11.2 variations in Chinese patients with development delay

Yanyan Zhao, Yuan-yuan Zhang, Xiaoliang Liu, 2021, BMC medical genomics.

Overexpression of cytochrome P450 4F2 in mice increases 20-hydroxyeicosatetraenoic acid production and arterial blood pressure.

Yanyan Zhao, Yuan-yuan Zhang, Xiang-Hong Yang, 2009, Kidney international.

Nonsense suppression induced readthrough of a novel PAX6 mutation in patient‐derived cells of congenital aniridia

Bijun Zhang, Yuan-yuan Zhang, Chuang Qiu, 2020, Molecular genetics & genomic medicine.

Genotype-phenotype correlation in 75 patients with small supernumerary marker chromosomes

Haiquan Sang, Yanyan Zhao, Yuan-yuan Zhang, 2020, Molecular Cytogenetics.

Human with-no-lysine kinase-4 3'-UTR acting as the enhancer and being targeted by miR-296.

Yanyan Zhao, Yuan-yuan Zhang, J. Mao, 2010, The international journal of biochemistry & cell biology.

R75Q de novo dominant mutation of GJB2 in a Chinese family with hearing loss and palmoplantar keratoderma.

Yuan-yuan Zhang, Z. Di, Dan-Qin Huang, 2014, International journal of pediatric otorhinolaryngology.

[Chromosomal abnormality diagnosis of male infertility by QF-PCR].

Yan-Yan Zhao, Yuan-yuan Zhang, Man-long Qi, 2011, Yi chuan = Hereditas.

Evaluation of non‐invasive prenatal testing to detect chromosomal aberrations in a Chinese cohort

Yanyan Zhao, Yuan-yuan Zhang, Wanting Cui, 2019, Journal of cellular and molecular medicine.

Keratin 9 L164P mutation in a Chinese pedigree with epidermolytic palmoplantar keratoderma, cytokeratin analysis, and literature review

Yanyan Zhao, Yuan-yuan Zhang, Chuang Qiu, 2019, Molecular genetics & genomic medicine.

Identification of Biomarkers of Autophagy-Related Genes Between Early and Advanced Carotid Atherosclerosis

Yuan-yuan Zhang, He Zhang, 2022, International journal of general medicine.

A Microdeletion of Chromosome 9q33.3 Encompasses the Entire LMX1B Gene in a Chinese Family with Nail Patella Syndrome

Yanyan Zhao, Yuan-yuan Zhang, Dan-Qin Huang, 2014, International Journal of Molecular Sciences.