Catarina Inês Gonçalves

3PUBLICATIONS
9CO-AUTHORS
Genetics not elsewhere classifiedEpigenetics (incl. genome methylation and epigenomics)Cancer genetics
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Publications (3)

|Nov 27, 2024
Kallmann Syndrome: Functional Analysis of a CHD7 Missense Variant Shows Aberrant RNA Splicing.

Josianne Nunes Carriço, Catarina Inês Gonçalves, José Maria Aragüés

|Oct 14, 2022
A Common Variant in the CDK8 Gene Is Associated with Sporadic Pituitary Adenomas in the Portuguese Population: A Case-Control Study.

Leonor M Gaspar, Catarina I Gonçalves, Fernando Fonseca

|Apr 23, 2022
A Novel FGFR1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism.

Lúcia Fadiga, Mariana Lavrador, Nuno Vicente

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