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Guillermo Pacheco-Cuellar

Showing results (1-10 of 4) with videos related to

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World Neurosurgery|May 13, 2022
Primary Benign Tumors of the Spinal CanalJosé Alberto Carlos-Escalante, Ángel Antonio Paz-López, Bernardo Cacho-Díaz, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 13, 2010
Noonan syndrome: prenatal diagnosis in a woman carrying a PTPN11 gene mutationNorma Celia González-Huerta, Juan Manuel Valdés-Miranda, Adrián Pérez-Cabrera, et al.
Current Eye Research|April 23, 2014
ADRB1 and ADBR2 gene polymorphisms and the ocular hypotensive response to topical betaxolol in healthy Mexican subjectsOlga Messina Baas, Guillermo Pacheco Cuellar, Jaime Toral-López, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2020
DOORS syndrome and a recurrent truncating ATP6V1B2 variantEliane Beauregard-Lacroix, Guillermo Pacheco-Cuellar, Norbert F Ajeawung, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
World Neurosurgery|May 13, 2022
Primary Benign Tumors of the Spinal CanalJosé Alberto Carlos-Escalante, Ángel Antonio Paz-López, Bernardo Cacho-Díaz, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 13, 2010
Noonan syndrome: prenatal diagnosis in a woman carrying a PTPN11 gene mutationNorma Celia González-Huerta, Juan Manuel Valdés-Miranda, Adrián Pérez-Cabrera, et al.
Current Eye Research|April 23, 2014
ADRB1 and ADBR2 gene polymorphisms and the ocular hypotensive response to topical betaxolol in healthy Mexican subjectsOlga Messina Baas, Guillermo Pacheco Cuellar, Jaime Toral-López, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2020
DOORS syndrome and a recurrent truncating ATP6V1B2 variantEliane Beauregard-Lacroix, Guillermo Pacheco-Cuellar, Norbert F Ajeawung, et al.
Pageof 1