Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrumAnne Thorwarth, Heiko Krude, Sabine Jyrch et al.|Journal of Medical Genetics|2014Cited by 114
Screening Chromosomal Aberrations by Array Comparative Genomic Hybridization in 80 Patients with Congenital Hypothyroidism and Thyroid DysgenesisAnne Thorwarth, Reinhard Ullmann, Ines Mueller et al.|The Journal of Clinical Endocrinology & Metabolism|2010Cited by 31