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Canadian Journal of Microbiology|July 1, 1994
Excision and transposition of Tn5 upon insertion in the hha gene of Escherichia coliC Badenas, C Madrid, A Juárez
Canadian Journal of Microbiology|June 1, 1994
Isolation and characterization of a Tn5-induced tolQ mutant of Escherichia coliC Madrid, C Badenas, A Juárez
Pediatric Cardiology|July 2, 2005
Elastin mutation screening in a group of patients affected by vascular abnormalitiesL Rodriguez-Revenga, C Badenas, A Carrió, et al.
The British Journal of Dermatology|April 19, 2016
Late-onset cutaneous porphyria in a patient heterozygous for a uroporphyrinogen III synthase gene mutationP Aguilera, C Badenas, S D Whatley, et al.
Clinical Genetics|November 15, 2002
SCA8 in the Spanish population including one homozygous patientB Tazón, C Badenas, L Jiménez, et al.
Journal of Intellectual Disability Research : JIDR|February 12, 2008
Deletion of the OPHN1 gene detected by aCGHI Madrigal, L Rodríguez-Revenga, C Badenas, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 4, 1999
Influence of the ACE gene polymorphism in the progression of renal failure in autosomal dominant polycystic kidney diseaseL Pérez-Oller, R Torra, C Badenas, et al.
Kidney International|July 1, 1997
Autosomal dominant polycystic kidney disease with anticipation and Caroli's disease associated with a PKD1 mutation. Rapid communicationR Torra, C Badenas, A Darnell, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 8, 1999
Autosomal recessive Alport syndrome: linkage analysis and clinical features in two familiesR Torra, C Badenas, F Cofán, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|June 15, 2000
[Heterozygosity loss and somatic mutations in type I and II dominant autosomal renal polycystic kidney disease: evidence of a recessive mechanism at a cell level in cystogenesis]L Pérez-Oller, R Torra, C Badenas, et al.
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