Molecular Cytogenetics
Official journal of
Articles
Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype
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
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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