Associated Papers
Genetic Analyses in a Cohort of Pediatric Patients with Congenital Hypothyroidism Based on Congenital Hypothyroidism Consensus Guideline.
Kurnaz E et al.
Hormone Research in Paediatrics, 2026
Respiratory and other organ manifestations in NKX2-1-related disorders: a systematic review.
Michel K et al.
Frontiers in Medicine, 2025
40395234 (PubMed )
Supplement: Data_Sheet_1.xlsx › Basal_characteristics
Advancing Cancer Care in Colombia: Results of the First In Situ Implementation of Comprehensive Genomic Profiling.
López Rivera JJ et al.
Journal of Personalized Medicine, 2024
39338229 (PubMed )
Supplement: jpm-14-00975-s001.zip › SUPPLEMENTARY_DATA.xlsx › Table_S2
Heterogeneity of lung disease associated with NK2 homeobox 1 mutations.
Nattes E et al.
Respiratory Medicine, 2017
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