Claudia Barletta-Carrillo

Evaluation of mitogenome sequence concordance, heteroplasmy detection, and haplogrouping in a worldwide lineage study using the Precision ID mtDNA Whole Genome Panel.

W. Parson, R. Lagacé, B. Budowle, 2019, Forensic science international. Genetics.

From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America

P. Møller, E. Hovig, P. Ashton-Prolla, 2018, International journal of cancer.

Evaluation of germline RET proto-oncogene variants in Peruvian patients with medullary thyroid carcinoma

S. Casavilca-Zambrano, Claudia Barletta-Carrillo, J. A. Poterico, 2020, Revista M�dica del Hospital General de M�xico.

[Lynch syndrome: genetic, clinical and diagnostic aspects].

Claudia Barletta-Carrillo, Maria del Carmen Castro-Mujica, María del Carmen Castro-Mujica, 2018, Revista de gastroenterologia del Peru : organo oficial de la Sociedad de Gastroenterologia del Peru.

Peruvian Newborn Male with 3p13 Deletion Syndrome Encompassing the FOXP1 Gene: Review of the Literature

Claudia Barletta-Carrillo, H. Abarca-Barriga, Milana Trubnykova, 2020, Journal of Pediatric Genetics.

A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America

P. Møller, E. Hovig, R. Reis, 2017, BMC Cancer.

[Nevoid basal-cell carcinoma syndrome (Gorlin Syndrome): report of two cases and review of the literature].

Claudia Barletta-Carrillo, M. D. L. Cruz, M. Castro-Mujica, 2017, Revista peruana de medicina experimental y salud publica.