Associated Papers
The interplay of mutagenesis and ecDNA shapes urothelial cancer evolution.
Nguyen DD et al.
Nature, 2024
39385020 (PubMed )
Supplement: 41586_2024_7955_MOESM11_ESM.xlsx › Figure_3e
Mutational Landscape Screening Through Comprehensive In Silico Analysis for Polycystic Ovarian Syndrome-Related Genes.
Dhar S et al.
Reproductive Sciences (thousand Oaks, Calif.), 2022
Androgen receptor gene mutations in 258 Han Chinese patients with polycystic ovary syndrome.
Tian L et al.
Experimental and Therapeutic Medicine, 2021
[Methyl-CpG-binding protein 2 gene and CDKL5 gene mutation in patients with Rett syndrome: analysis of 177 Chinese pediatric patients].
Li MR et al.
Zhonghua Yi Xue Za Zhi, 2009
[Correlation between MECP2 genotype and phenotype in Chinese patients with Rett syndrome].
Li MR et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2009
MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome.
Li MR et al.
Journal of Human Genetics, 2007
[MECP2 gene mutations in twenty-six cases with atypical Rett syndrome].
Li MR et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2006
[Clinical feature of Rett syndrome and MeCP2 genotype/phenotype correlation analysis].
Bao XH et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2004
Preserved speech variants of the Rett syndrome: molecular and clinical analysis.
Zappella M et al.
American Journal of Medical Genetics, 2001
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