Associated Papers
Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+).
Rivera-Munoz EA et al.
European Journal of Human Genetics : Ejhg, 2025
40913078 (PubMed )
Supplement: NIHMS2114636-supplement-Supplemental_Table_S1.xlsx › Table_S1
FGFR3 overexpression is a useful detection tool for FGFR3 fusions and sequence variations in glioma.
Schittenhelm J et al.
Neuro-oncology Practice, 2021
Review: Balancing Selection for Deleterious Alleles in Livestock.
Derks MFL et al.
Frontiers in Genetics, 2021
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