Gildardo Zafra

A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca ²⁺ release channel function and severe central core disease

Patrick J. Lynch, Jiefei Tong, M Lehane et al. · Proceedings of the National Academy of Sciences · 1999 · 234 citations

Life Sciences, Genetics, Physiology +17

Microsatellite analysis in Turner syndrome: Parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes

Nancy Monroy‐Jaramillo, Marisol López, Alicia Cervantes et al. · American Journal of Medical Genetics · 2001 · 22 citations

Life Sciences, Genetics, Molecular Genetics +17

PCR–PRINS–FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype

Alicia Cervantes, Roberto Guevara-Yañez, Marisol López et al. · Clinical Genetics · 2001 · 10 citations

Life Sciences, Genetics, Molecular Genetics +17