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- [3] NKX2-1 homeobox gene, brain-lung-thyroid syndrome: a case study AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2024, 367 : S302 - S302
- [5] NKX2-1 mutations in brain-lung-thyroid syndrome: a case series of four patients JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2014, 27 (3-4): : 373 - 378
- [6] NKX2-1 GENE DEFECTS IN A PEDIATRIC COHORT WITH SUSPECTED BRAIN-LUNG-THYROID SYNDROME HORMONE RESEARCH IN PAEDIATRICS, 2017, 88 : 376 - 377
- [7] Haploinsufficiency of NKX2-1 in Brain-Lung-Thyroid Syndrome with Additional Multiple Pituitary Dysfunction HORMONE RESEARCH IN PAEDIATRICS, 2020, 92 (05): : 340 - 344
- [9] Is Benign Hereditary Chorea Really Benign? Brain-Lung-Thyroid Syndrome Caused by NKX2-1 Mutations MOVEMENT DISORDERS CLINICAL PRACTICE, 2019, 6 (01): : 34 - 39
- [10] TAZ/WWTR1 Mediates the Pulmonary Effects of NKX2-1 Mutations in Brain-Lung-Thyroid Syndrome JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2018, 103 (03): : 839 - 852