Associated Papers
Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene.
Charng WL et al.
Journal of Medical Genetics, 2024
38663984 (PubMed )
Supplement: jmg-2024-109846supp001.xlsx › Table_S4
Whole-Exome Sequencing Reveals Clinical Potential of Circulating Tumor DNA from Peritoneal Fluid and Plasma in Endometrial Cancer.
Ju HY et al.
Cancers, 2022
35626111 (PubMed )
Supplement: cancers-14-02506-s001.zip › Supplementary_Tables.xlsx › Supplementary_Table_S2
Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.
Chen X et al.
Bmc Medical Genetics, 2019
31146700 (PubMed )
Supplement: 12881_2019_813_MOESM1_ESM.xls › CHD7_ChenXiang_query_Report_Fil
Genetic analysis of HOXA11 gene in Chinese patients with cryptorchidism.
Lu P et al.
Andrologia, 2018
Exome sequencing reveals a novel PTHLH mutation in a Chinese pedigree with brachydactyly type E and short stature.
Wang J et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2015
Select a paper to view details