Sonia Canún

Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome

Nikki Plaster, Rabi Tawil, Martin Tristani‐Firouzi et al. · Cell · 2001 · 998 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Idiopathic multicentric osteolysis with facial anomalies and nephropathy

Alessandra Carnevale, Sonia Canún, Luciano Mendoza et al. · American Journal of Medical Genetics · 1987 · 30 citations

Medicine, Nephrology, Radiology +14

Absent tibiae, triphalangeal thumbs and polydactyly: description of a family and prenatal diagnosis

Sonia Canún, Rosa Maria Lomeli, R. Ocampo Martínez et al. · Clinical Genetics · 1984 · 22 citations

Medicine, Anatomy, Genetics +8

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

Videonasopharyngoscopy in patients with 22q11.2 deletion syndrome (Shprintzen syndrome)

Antonio Ysunza, Ma. Carmen Pamplona, Sonia Canún et al. · International Journal of Pediatric Otorhinolaryngology · 2003 · 19 citations

Medicine, Otolaryngology, Pediatric Genetics +8