Search

Search Constraints

You searched for: Author/Creator Correa, Fernanda A.

Search Results

2. Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes. (10th January 2018)

3. Relatively high frequency of non‐synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly. (12th March 2013)