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Winnie Schröder

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

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Hamostaseologie|September 28, 2018
Diagnostic Single Gene Analyses Beyond SangerJuliane Najm, Matthias Rath, Winnie Schröder, et al.
Neurosurgical Review|June 1, 2013
Predictive genetic testing of at-risk relatives requires analysis of all CCM genes after identification of an unclassified CCM1 variant in an individual affected with cerebral cavernous malformationsWinnie Schröder, Juliane Najm, Stefanie Spiegler, et al.
Revista De Biologia Tropical|May 7, 2008
Common polymorphisms and cardiovascular factors in patients with myocardial infarction of Costa RicaLizbeth Salazar-Sánchez, Lilliana Chaves, Mayra Cartin, et al.
American Journal of Human Biology : the Official Journal of the Human Biology Council|December 23, 2003
Prevalence of eight molecular markers associated with thrombotic diseases in six Amerindian tribes and two African groups of Costa RicaFalko H Herrmann, Lizbeth Salazar-Sánchez, Gudrun Schuster, et al.
Cell Biochemistry and Function|January 2, 2007
The FXIIIVal34Leu, common and risk factors of venous thrombosis in early middle-age Costa Rican patientsLizbeth Salazar-Sánchez, Maria Paz Leon, Mayra Cartin, et al.
Revista De Biologia Tropical|March 17, 2007
Molecular diagnosis of hemophilia A and B. Report of five families from Costa RicaLizbeth Salazar-Sánchez, Guillermo Jiménez-Cruz, Pilar Chaverri, et al.
Pharmacogenetics|May 2, 2003
Platelet receptor and clotting factor polymorphisms as genetic risk factors for thromboembolic complications in heparin-induced thrombocytopeniaLena E Carlsson, Norbert Lubenow, Carmen Blumentritt, et al.
European Journal of Human Genetics : EJHG|October 31, 2013
New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation updateClaire Laure Navarro, Vera Esteves-Vieira, Sébastien Courrier, et al.
Molecular Genetics & Genomic Medicine|April 2, 2014
High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one-third of probands are minorsStefanie Spiegler, Juliane Najm, Jian Liu, et al.
Pageof 1

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

Sort By:
Pageof 1
Hamostaseologie|September 28, 2018
Diagnostic Single Gene Analyses Beyond SangerJuliane Najm, Matthias Rath, Winnie Schröder, et al.
Neurosurgical Review|June 1, 2013
Predictive genetic testing of at-risk relatives requires analysis of all CCM genes after identification of an unclassified CCM1 variant in an individual affected with cerebral cavernous malformationsWinnie Schröder, Juliane Najm, Stefanie Spiegler, et al.
Revista De Biologia Tropical|May 7, 2008
Common polymorphisms and cardiovascular factors in patients with myocardial infarction of Costa RicaLizbeth Salazar-Sánchez, Lilliana Chaves, Mayra Cartin, et al.
American Journal of Human Biology : the Official Journal of the Human Biology Council|December 23, 2003
Prevalence of eight molecular markers associated with thrombotic diseases in six Amerindian tribes and two African groups of Costa RicaFalko H Herrmann, Lizbeth Salazar-Sánchez, Gudrun Schuster, et al.
Cell Biochemistry and Function|January 2, 2007
The FXIIIVal34Leu, common and risk factors of venous thrombosis in early middle-age Costa Rican patientsLizbeth Salazar-Sánchez, Maria Paz Leon, Mayra Cartin, et al.
Revista De Biologia Tropical|March 17, 2007
Molecular diagnosis of hemophilia A and B. Report of five families from Costa RicaLizbeth Salazar-Sánchez, Guillermo Jiménez-Cruz, Pilar Chaverri, et al.
Pharmacogenetics|May 2, 2003
Platelet receptor and clotting factor polymorphisms as genetic risk factors for thromboembolic complications in heparin-induced thrombocytopeniaLena E Carlsson, Norbert Lubenow, Carmen Blumentritt, et al.
European Journal of Human Genetics : EJHG|October 31, 2013
New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation updateClaire Laure Navarro, Vera Esteves-Vieira, Sébastien Courrier, et al.
Molecular Genetics & Genomic Medicine|April 2, 2014
High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one-third of probands are minorsStefanie Spiegler, Juliane Najm, Jian Liu, et al.
Pageof 1