Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M García-Hoyos

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 14, 2016
Diverging results of areal and volumetric bone mineral density in Down syndromeM García-Hoyos, M T García-Unzueta, D de Luis, et al.
Human Genetics|October 11, 2008
Gene symbol: RPGR. Disease: Retinitis PigmentosaAscensión Giménez, R Riveiro, M J Trujillo-Tiebas, et al.
Human Genetics|June 29, 2007
Gene symbol: RP2Cristina Villaverde-Montero, M García-Hoyos, A Giménez-Pardo, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
New approach for the refinement of the location of the X-chromosome breakpoint in a previously described female patient with choroideremia carrying a X;4 translocationM García-Hoyos, R Sanz, D Diego-Alvarez, et al.
Human Genetics|October 11, 2008
Gene symbol: CHM. Disease: ChoroideraemiaCristina Villaverde, M J Trujillo-Tiebas, M A López-Martinez, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|June 28, 2018
Abnormal bone turnover in individuals with low serum alkaline phosphataseL López-Delgado, L Riancho-Zarrabeitia, M T García-Unzueta, et al.
Prenatal Diagnosis|March 11, 2003
Huntington disease-unaffected fetus diagnosed from maternal plasma using QF-PCRM C González-González, M J Trujillo, M Rodríguez de Alba, et al.
Prenatal Diagnosis|October 16, 2002
Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasmaM C González-González, M García-Hoyos, M J Trujillo, et al.
Neuromuscular Disorders : NMD|January 20, 2016
Long-term follow-up in patients with congenital myasthenic syndrome due to RAPSN mutationsD Natera-de Benito, M Bestué, J J Vilchez, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 14, 2016
Diverging results of areal and volumetric bone mineral density in Down syndromeM García-Hoyos, M T García-Unzueta, D de Luis, et al.
Human Genetics|October 11, 2008
Gene symbol: RPGR. Disease: Retinitis PigmentosaAscensión Giménez, R Riveiro, M J Trujillo-Tiebas, et al.
Human Genetics|June 29, 2007
Gene symbol: RP2Cristina Villaverde-Montero, M García-Hoyos, A Giménez-Pardo, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
New approach for the refinement of the location of the X-chromosome breakpoint in a previously described female patient with choroideremia carrying a X;4 translocationM García-Hoyos, R Sanz, D Diego-Alvarez, et al.
Human Genetics|October 11, 2008
Gene symbol: CHM. Disease: ChoroideraemiaCristina Villaverde, M J Trujillo-Tiebas, M A López-Martinez, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|June 28, 2018
Abnormal bone turnover in individuals with low serum alkaline phosphataseL López-Delgado, L Riancho-Zarrabeitia, M T García-Unzueta, et al.
Prenatal Diagnosis|March 11, 2003
Huntington disease-unaffected fetus diagnosed from maternal plasma using QF-PCRM C González-González, M J Trujillo, M Rodríguez de Alba, et al.
Prenatal Diagnosis|October 16, 2002
Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasmaM C González-González, M García-Hoyos, M J Trujillo, et al.
Neuromuscular Disorders : NMD|January 20, 2016
Long-term follow-up in patients with congenital myasthenic syndrome due to RAPSN mutationsD Natera-de Benito, M Bestué, J J Vilchez, et al.
Pageof 1