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Showing results (101-110 of 122) with videos related to

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Genetic Counseling (Geneva, Switzerland)|August 8, 2009
Chromosome instability in a patient with recurrent abortionsL Bobadilla-Morales, M I Cervantes-Luna, T A García-Cobián, et al.
Genetic Counseling (Geneva, Switzerland)|April 25, 2013
Dysgnathia complex sine holoprosencephaly nor synotia: a case report and discussion of its nosologyJ R Corona-Rivera, S A Trujillo-Ponce, E Barrios-Prieto, et al.
Minerva Ginecologica|February 12, 2011
[Prevention of postoperative abdominal adhesions in gynecological surgery. Consensus paper of an Italian gynecologists' task force on adhesions]V Mais, R Angioli, E Coccia, et al.
Dalton Transactions (Cambridge, England : 2003)|January 17, 2017
Chiral bidentate [N,S]-ferrocene ligands based on a thiazoline framework. Synthesis and use in palladium-catalyzed asymmetric allylic alkylationE P Sánchez-Rodríguez, F Hochberger-Roa, R Corona-Sánchez, et al.
Genetic Counseling (Geneva, Switzerland)|May 23, 2007
SED-brachydactyly and distinctive speech: report of two new casesD García-Cruz, G F Zafra de la Rosa, J Sánchez-Corona, et al.
Microorganisms|February 27, 2026
Siderophore-Producing Bacteria from the Santiago River: A Quantitative Study and Biocomposite ApplicationsMariana R Corona-Ramírez, Nidia N García-Valdez, Luis A Romero-Cano, et al.
Boletin Medico Del Hospital Infantil De Mexico|December 8, 2022
Frequency of chromosome 22q11.2 deletion among newborns with non-syndromic congenital heart defects from western MexicoGerardo E Fabián-Morales, Lucina Bobadilla-Morales, Christian Peña-Padilla, et al.
Journal of the American Pharmacists Association : Japha|October 10, 2017
Residency pathways to ambulatory care practice: Essential insights for students, residents, and educatorsSarah M Westberg, Stuart J Beatty, Andrea R Corona, et al.
Clinical Genetics|November 23, 2016
Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathyC Peña-Padilla, C R Marshall, S Walker, et al.
The British Journal of Dermatology|February 1, 2006
Three-point checklist of dermoscopy: an open internet studyI Zalaudek, G Argenziano, H P Soyer, et al.
Pageof 13

Showing results (101-110 of 122) with videos related to

Sort By:
Pageof 13
Genetic Counseling (Geneva, Switzerland)|August 8, 2009
Chromosome instability in a patient with recurrent abortionsL Bobadilla-Morales, M I Cervantes-Luna, T A García-Cobián, et al.
Genetic Counseling (Geneva, Switzerland)|April 25, 2013
Dysgnathia complex sine holoprosencephaly nor synotia: a case report and discussion of its nosologyJ R Corona-Rivera, S A Trujillo-Ponce, E Barrios-Prieto, et al.
Minerva Ginecologica|February 12, 2011
[Prevention of postoperative abdominal adhesions in gynecological surgery. Consensus paper of an Italian gynecologists' task force on adhesions]V Mais, R Angioli, E Coccia, et al.
Dalton Transactions (Cambridge, England : 2003)|January 17, 2017
Chiral bidentate [N,S]-ferrocene ligands based on a thiazoline framework. Synthesis and use in palladium-catalyzed asymmetric allylic alkylationE P Sánchez-Rodríguez, F Hochberger-Roa, R Corona-Sánchez, et al.
Genetic Counseling (Geneva, Switzerland)|May 23, 2007
SED-brachydactyly and distinctive speech: report of two new casesD García-Cruz, G F Zafra de la Rosa, J Sánchez-Corona, et al.
Microorganisms|February 27, 2026
Siderophore-Producing Bacteria from the Santiago River: A Quantitative Study and Biocomposite ApplicationsMariana R Corona-Ramírez, Nidia N García-Valdez, Luis A Romero-Cano, et al.
Boletin Medico Del Hospital Infantil De Mexico|December 8, 2022
Frequency of chromosome 22q11.2 deletion among newborns with non-syndromic congenital heart defects from western MexicoGerardo E Fabián-Morales, Lucina Bobadilla-Morales, Christian Peña-Padilla, et al.
Journal of the American Pharmacists Association : Japha|October 10, 2017
Residency pathways to ambulatory care practice: Essential insights for students, residents, and educatorsSarah M Westberg, Stuart J Beatty, Andrea R Corona, et al.
Clinical Genetics|November 23, 2016
Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathyC Peña-Padilla, C R Marshall, S Walker, et al.
The British Journal of Dermatology|February 1, 2006
Three-point checklist of dermoscopy: an open internet studyI Zalaudek, G Argenziano, H P Soyer, et al.
Pageof 13