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2. Familial deletion of the HOXA gene cluster associated with Hand–Foot–Genital syndrome and phenotypic variability. Issue 1 (20th September 2016)

3. Guidelines for the Development of Comprehensive Care Centers for Congenital Adrenal Hyperplasia: Guidance from the CARES Foundation Initiative. (11th November 2010)

4. Identification of Unique, Heterozygous Germline Mutation, STK11 (p.F354L), in a Child with an Encapsulated Follicular Variant of Papillary Thyroid Carcinoma within Six Months of Completing Treatment for Neuroblastoma. (July 2015)