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P Carbonell

Showing results (31-40 of 42) with videos related to

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European Journal of Trauma and Emergency Surgery : Official Publication of the European Trauma Society|January 28, 2016
Limb amputation among patients with surgically treated popliteal arterial injury: analysis of 15 years of experience in an urban trauma center in Cali, ColombiaA F García, Á I Sánchez, M Millán, et al.
Anales Espanoles De Pediatria|March 1, 1996
[A genetic and molecular study of 85 families affected with the fragile X syndrome]M Milà Recasens, A Sánchez Díaz, G Glover López, et al.
Journal of Medical Genetics|March 1, 1995
FRAXE and mental retardationJ C Mulley, S Yu, D Z Loesch, et al.
International Journal of Cancer|January 31, 2012
Colorectal serrated adenocarcinoma shows a different profile of oncogene mutations, MSI status and DNA repair protein expression compared to conventional and sporadic MSI-H carcinomasJ García-Solano, P Conesa-Zamora, P Carbonell, et al.
Revista Medica De Chile|September 30, 2003
[Frequency of abdominal aortic aneurysms in adult population with known risk factors]Francisco Valdés, Nelson Sepúlveda, Albrecht Krämer, et al.
Medical Hypotheses|April 13, 2020
When genetic and surname analyses meet historical sources: The C56R mutation associated with factor XI deficiency as a marker of human migration during the Spanish ReconquistaF Bauduer, M E de la Morena-Barrio, S Salloum-Asfar, et al.
Medicina Clinica|June 22, 1999
[Genetic analysis of RET mutations in families with multiple endocrine neoplasia type II in the community of Murcia]F J Pomares Gómez, M J Bernabé Espinosa, X Matías-Guiu Guía, et al.
Alimentary Pharmacology & Therapeutics|April 12, 2000
Interferon alfa-2b plus ribavirin for chronic hepatitis C patients who have not responded to interferon monotherapyO Lo Iacono, A Castro, M Diago, et al.
Neuromuscular Disorders : NMD|September 1, 2018
A novel MYH7 founder mutation causing Laing distal myopathy in Southern SpainP Carbonell-Corvillo, E Tristán-Clavijo, M Cabrera-Serrano, et al.
American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
European Journal of Trauma and Emergency Surgery : Official Publication of the European Trauma Society|January 28, 2016
Limb amputation among patients with surgically treated popliteal arterial injury: analysis of 15 years of experience in an urban trauma center in Cali, ColombiaA F García, Á I Sánchez, M Millán, et al.
Anales Espanoles De Pediatria|March 1, 1996
[A genetic and molecular study of 85 families affected with the fragile X syndrome]M Milà Recasens, A Sánchez Díaz, G Glover López, et al.
Journal of Medical Genetics|March 1, 1995
FRAXE and mental retardationJ C Mulley, S Yu, D Z Loesch, et al.
International Journal of Cancer|January 31, 2012
Colorectal serrated adenocarcinoma shows a different profile of oncogene mutations, MSI status and DNA repair protein expression compared to conventional and sporadic MSI-H carcinomasJ García-Solano, P Conesa-Zamora, P Carbonell, et al.
Revista Medica De Chile|September 30, 2003
[Frequency of abdominal aortic aneurysms in adult population with known risk factors]Francisco Valdés, Nelson Sepúlveda, Albrecht Krämer, et al.
Medical Hypotheses|April 13, 2020
When genetic and surname analyses meet historical sources: The C56R mutation associated with factor XI deficiency as a marker of human migration during the Spanish ReconquistaF Bauduer, M E de la Morena-Barrio, S Salloum-Asfar, et al.
Medicina Clinica|June 22, 1999
[Genetic analysis of RET mutations in families with multiple endocrine neoplasia type II in the community of Murcia]F J Pomares Gómez, M J Bernabé Espinosa, X Matías-Guiu Guía, et al.
Alimentary Pharmacology & Therapeutics|April 12, 2000
Interferon alfa-2b plus ribavirin for chronic hepatitis C patients who have not responded to interferon monotherapyO Lo Iacono, A Castro, M Diago, et al.
Neuromuscular Disorders : NMD|September 1, 2018
A novel MYH7 founder mutation causing Laing distal myopathy in Southern SpainP Carbonell-Corvillo, E Tristán-Clavijo, M Cabrera-Serrano, et al.
American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.
Pageof 5