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Harry Pachajoa

Showing results (1-10 of 126) with videos related to

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Medicina|April 17, 2014
[Hereditary multiple exostosis]Harry Pachajoa
Archivos Argentinos De Pediatria|November 22, 2016
[Deletion on the short arm of chromosome 18 syndrome diagnosed by array comparative genomic hybridization. Presentation of one case with a mild phenotype]Harry Pachajoa
Archivos Argentinos De Pediatria|August 6, 2013
[Double aneuploidy (trisomy X, trisomy 18) in a newborn with trisomy 18 phenotype]Harry Pachajoa
Archivos Argentinos De Pediatria|July 5, 2012
[Isotretinoin embryopathy with microtia-anotia and congenital heart disease: case report]Harry Pachajoa, Adriana Ordoñez
American Journal of Medical Genetics. Part A|May 26, 2012
Sirenomelia and cyclopia in the same patient after a cluster of cyclopia and sirenomelia in Cali (South America)Harry Pachajoa, Carolina Isaza
American Journal of Medical Genetics. Part A|August 5, 2011
Possible case of sirenomelia in the Tumaco-Tolita pottery pre-Columbian culture, 2000 years before the epidemic focus of sirenomelia in Cali-ColombiaHarry Pachajoa, Carlos Rodriguez
Orthopedic Research and Reviews|December 5, 2022
A Patient with Bone Fragility, Multiple Fractures, Osteosarcoma, and the Variant c.143A>G in the <i>IFITM5</i> Gene: A Case ReportHarry Pachajoa, Sebastian Giraldo-Ocampo
Journal of Medical Case Reports|July 28, 2016
Deletion 21q22.3 and duplication 7q35q36.3 in a Colombian girl: a case reportFelipe Ruiz-Botero, Harry Pachajoa
Orphanet Journal of Rare Diseases|October 15, 2025
Recent advances in mucopolysaccharidosis IVA treatmentAndrés Felipe Leal, Harry Pachajoa
Colombia Medica (Cali, Colombia)|June 7, 2019
Wiedemann-Steiner syndrome with a novel pathogenic variant in KMT2A: a case reportDiana Ramirez-Montaño, Harry Pachajoa
Pageof 13

Showing results (1-10 of 126) with videos related to

Sort By:
Pageof 13
Medicina|April 17, 2014
[Hereditary multiple exostosis]Harry Pachajoa
Archivos Argentinos De Pediatria|November 22, 2016
[Deletion on the short arm of chromosome 18 syndrome diagnosed by array comparative genomic hybridization. Presentation of one case with a mild phenotype]Harry Pachajoa
Archivos Argentinos De Pediatria|August 6, 2013
[Double aneuploidy (trisomy X, trisomy 18) in a newborn with trisomy 18 phenotype]Harry Pachajoa
Archivos Argentinos De Pediatria|July 5, 2012
[Isotretinoin embryopathy with microtia-anotia and congenital heart disease: case report]Harry Pachajoa, Adriana Ordoñez
American Journal of Medical Genetics. Part A|May 26, 2012
Sirenomelia and cyclopia in the same patient after a cluster of cyclopia and sirenomelia in Cali (South America)Harry Pachajoa, Carolina Isaza
American Journal of Medical Genetics. Part A|August 5, 2011
Possible case of sirenomelia in the Tumaco-Tolita pottery pre-Columbian culture, 2000 years before the epidemic focus of sirenomelia in Cali-ColombiaHarry Pachajoa, Carlos Rodriguez
Orthopedic Research and Reviews|December 5, 2022
A Patient with Bone Fragility, Multiple Fractures, Osteosarcoma, and the Variant c.143A>G in the <i>IFITM5</i> Gene: A Case ReportHarry Pachajoa, Sebastian Giraldo-Ocampo
Journal of Medical Case Reports|July 28, 2016
Deletion 21q22.3 and duplication 7q35q36.3 in a Colombian girl: a case reportFelipe Ruiz-Botero, Harry Pachajoa
Orphanet Journal of Rare Diseases|October 15, 2025
Recent advances in mucopolysaccharidosis IVA treatmentAndrés Felipe Leal, Harry Pachajoa
Colombia Medica (Cali, Colombia)|June 7, 2019
Wiedemann-Steiner syndrome with a novel pathogenic variant in KMT2A: a case reportDiana Ramirez-Montaño, Harry Pachajoa
Pageof 13