M. C. González-González

Next generation sequencing for rapid diagnosis of a rare early onset spastic paraplegia: A novel pathological variant in FA2H gene

F. Cava, M. C. González-González, M. Gutiérrez, 2018, Revista del Laboratorio Clínico.

Huntington disease–unaffected fetus diagnosed from maternal plasma using QF‐PCR

C. Ayuso, M. García-Hoyos, C. Ramos, 2003, Prenatal diagnosis.

Improvement in strategies for the non-invasive prenatal diagnosis of Huntington disease

C. Ayuso, M. García-Hoyos, M. Trujillo-Tiebas, 2008, Journal of Assisted Reproduction and Genetics.

Early Huntington disease prenatal diagnosis by maternal semiquantitative fluorescent-PCR

C. Ramos, C. Ramos, M. Rodríguez de Alba, 2003, Neurology.

Cryptic 6q subtelomeric deletion associated with a paracentric inversion in a mildly retarded child.

C. Ayuso, C. Ramos, I. Lorda‐Sánchez, 2000, American journal of medical genetics.

Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasma

C. Ayuso, M. García-Hoyos, C. Ramos, 2002, Prenatal diagnosis.

Chromosomal Mosaicism for Isochromosome 11q Confined to CVS Direct Preparations

C. Ayuso, M. Robledo, C. Ramos, 2001, Fetal Diagnosis and Therapy.