Molecular Cytogenetics
Articles
Clinical, cytogenetic, and molecular findings of isodicentric Y chromosomes
Laundering CNV data for candidate process prioritization in brain disorders
A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing
The variome concept: focus on CNVariome
A novel 14q13.1–21.1 deletion identified by CNV-Seq in a patient with brain-lung-thyroid syndrome, tooth agenesis and immunodeficiency
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