Associated Papers
3M syndrome with novel CUL7 variants in a Chinese patient: a case report.
Liu H et al.
Frontiers in Pediatrics, 2025
41234413 (PubMed )
Supplement: Table1.xlsx › Table_1
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.
Guo H et al.
Molecular Autism, 2018
30564305 (PubMed )
Supplement: 13229_2018_247_MOESM5_ESM.xlsx › LGD
Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variants.
Hu X et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2017
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