Associated Papers
Prenatal Exome Sequencing Analysis in Fetuses With Structural Anomalies: A Multicenter Prospective Cohort Study With Practical Implications.
Jiang Y et al.
Prenatal Diagnosis, 2026
Prenatal diagnosis of fetuses with region of homozygosity detected by single nucleotide polymorphism array: a retrospective cohort study.
Liang B et al.
Journal of Human Genetics, 2022
The human type I collagen mutation database.
Dalgleish R
Nucleic Acids Research, 1997
Select a paper to view details