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Harry Pachajoa

Showing results (11-20 of 126) with videos related to

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BMC Pediatrics|October 3, 2022
2q37 deletion syndrome in a Colombian patient with macrocephaly: a case reportSebastian Giraldo-Ocampo, Harry Pachajoa
Archivos Argentinos De Pediatria|July 12, 2016
[Langer-Giedion syndrome with 8q23.1-q24.12 deletion diagnosed by comparative genomic hybridization]Felipe Ruiz-Botero, Harry Pachajoa
Gaceta Medica De Mexico|November 26, 2011
[Diagnosis of prenantal holoprosencephalic agnatia complex]Harry Pachajoa, Juan Carlos Quintero
Medicina|April 24, 2012
[Cutis verticis gyrata]Paula M Hurtado, Harry Pachajoa
Colombia Medica (Cali, Colombia)|August 8, 2014
Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome) in the pre-Columbian culture of ColombiaHarry Pachajoa, Carlos Armando Rodriguez
Archives of Disease in Childhood. Fetal and Neonatal Edition|April 13, 2013
Holoprosencephaly with premaxillary agenesis in a prehistoric skullHarry Pachajoa, Carlos A Rodriguez
Congenital Anomalies|May 22, 2016
Syndromic microphthalmia-3 caused by a mutation on gene SOX2 in a Colombian male patientAndrés Felipe Ramirez-Botero, Harry Pachajoa
BMJ Case Reports|August 2, 2013
Mosaic trisomy 13 and a sacral appendageHarry Pachajoa, Luis Enrique Meza Escobar
BMJ Case Reports|June 10, 2015
Clinical and molecular characterisation of two siblings with fibrodysplasia ossificans progressiva, from the Colombian Pacific coast (South America)Harry Pachajoa, Andres Felipe Ramirez Botero
International Journal of Molecular Sciences|July 12, 2025
Mesenchymal Stem Cell-Derived Extracellular Vesicles: Seeking into Cell-Free Therapies for Bone-Affected Lysosomal Storage DisordersAndrés Felipe Leal, Harry Pachajoa, Shunji Tomatsu
Pageof 13

Showing results (11-20 of 126) with videos related to

Sort By:
Pageof 13
BMC Pediatrics|October 3, 2022
2q37 deletion syndrome in a Colombian patient with macrocephaly: a case reportSebastian Giraldo-Ocampo, Harry Pachajoa
Archivos Argentinos De Pediatria|July 12, 2016
[Langer-Giedion syndrome with 8q23.1-q24.12 deletion diagnosed by comparative genomic hybridization]Felipe Ruiz-Botero, Harry Pachajoa
Gaceta Medica De Mexico|November 26, 2011
[Diagnosis of prenantal holoprosencephalic agnatia complex]Harry Pachajoa, Juan Carlos Quintero
Medicina|April 24, 2012
[Cutis verticis gyrata]Paula M Hurtado, Harry Pachajoa
Colombia Medica (Cali, Colombia)|August 8, 2014
Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome) in the pre-Columbian culture of ColombiaHarry Pachajoa, Carlos Armando Rodriguez
Archives of Disease in Childhood. Fetal and Neonatal Edition|April 13, 2013
Holoprosencephaly with premaxillary agenesis in a prehistoric skullHarry Pachajoa, Carlos A Rodriguez
Congenital Anomalies|May 22, 2016
Syndromic microphthalmia-3 caused by a mutation on gene SOX2 in a Colombian male patientAndrés Felipe Ramirez-Botero, Harry Pachajoa
BMJ Case Reports|August 2, 2013
Mosaic trisomy 13 and a sacral appendageHarry Pachajoa, Luis Enrique Meza Escobar
BMJ Case Reports|June 10, 2015
Clinical and molecular characterisation of two siblings with fibrodysplasia ossificans progressiva, from the Colombian Pacific coast (South America)Harry Pachajoa, Andres Felipe Ramirez Botero
International Journal of Molecular Sciences|July 12, 2025
Mesenchymal Stem Cell-Derived Extracellular Vesicles: Seeking into Cell-Free Therapies for Bone-Affected Lysosomal Storage DisordersAndrés Felipe Leal, Harry Pachajoa, Shunji Tomatsu
Pageof 13