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1. Biallelic DNAJC3 variants in a neuroendocrine developmental disorder with insulin dysregulation. Issue 1 (15th October 2021)

2. Biallelic DNAJC3 variants in a neuroendocrine developmental disorder with insulin dysregulation. Issue 1 (January 2022)

3. Extending the phenotype associated with the CSNK2A1‐related Okur–Chung syndrome—A clinical study of 11 individuals. Issue 5 (31st January 2018)

4. J8 Two case studies demonstrating transmission of unstable huntington's disease intermediate alleles and the implications for genetic counselling practice. (13th September 2016)