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Autosomal Dominant Nanophthalmos and High Hyperopia Associated With a C-terminal Frameshift Variant in MYRF
Broadening the phenotype of LRP2 mutations
California Birth Defects Monitoring Program
Can Circular RNAs be Used as Prenatal Biomarkers for Congenital Diaphragmatic Hernia?
CBDMP
CDC NCEH Division of
Cell culture system to assay candidate genes and molecular pathways implicated in congenital diaphragmatic hernias
Clinical/Epidemiolog
Common Drugs and Che
Congenital Anomalies In The Teratological Collection Of Museum Vrolik In Amsterdam, The Netherlands. III: Primary Field Defects, Sequences, And Other Complex Anomalies.
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