Milagros M. Duenas-Roque

Haploinsufficiency of SF3B2 causes craniofacial microsomia

Gloria L. Porras-Hurtado, A. Drake, D. Chitayat, 2021, Nature Communications.

MLPA followed by target‐NGS to detect mutations in the dystrophin gene of Peruvian patients suspected of DMD/DMB

R. Fujita, A. Estrada-Cuzcano, Diana Rojas-Málaga, 2021, Molecular genetics & genomic medicine.

Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical Practice

Robert P. Carson, Robert C. Pedersen, Sean T. Hwang, 2022, JAMA neurology.

Turner syndrome in diverse populations

Yonit A. Addissie, A. Mégarbané, V. Dissanayake, 2019, American journal of medical genetics. Part A.

Genetics and genomics in Peru: Clinical and research perspective

J. M. Iglesias-Pedraz, H. Guio, R. Fujita, 2018, Molecular genetics & genomic medicine.

Novel mutation in ENG gene causing Hereditary Hemorrhagic Telangiectasia in a Peruvian family

R. Fujita, A. Zevallos-Morales, Milagros M Dueñas-Roque, 2020, Genetics and molecular biology.

Genetics and genomics in Peru: Clinical and research perspective

J. M. Iglesias-Pedraz, H. Guio, R. Fujita, 2018, Molecular genetics & genomic medicine.

[Factors associated with survival at one year of life in neonates with severe congenital cardiopathy in A National Hospital in Peru].

Hugo Arroyo-Hernández, Camilo E. Torres-Romucho, Victor G. Uriondo-Oré, 2019, Revista peruana de medicina experimental y salud publica.

New SHH and Known SIX3 Variants in a Series of Latin American Patients with Holoprosencephaly

D. Cavalcanti, M. Sanseverino, I. Orioli, 2021, Molecular Syndromology.