Associated Papers
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Riedhammer KM et al.
Kidney International, 2024
38154558 (PubMed )
Supplement: mmc2.xlsx › Family_1
Identification of Novel Candidate Genes for Familial Thyroid Cancer by Whole Exome Sequencing.
Tous C et al.
International Journal of Molecular Sciences, 2023
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