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C Stoll

Showing results (291-300 of 377) with videos related to

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American Journal of Medical Genetics. Part A|April 11, 2003
Prenatal detection of rare chromosomal autosomal abnormalities in EuropeN Baena, C De Vigan, E Cariati, et al.
Intensive Care Medicine|February 8, 2000
Effects of noninvasive positive pressure ventilatory support in non-COPD patients with acute respiratory insufficiency after early extubationE Kilger, J Briegel, M Haller, et al.
Annales De Genetique|January 1, 1996
A study on limb reduction defects in six European regionsC Stoll, E Calzolari, M Cornel, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Severe hypernatremic dehydration in an infant with Netherton syndromeC Stoll, Y Alembik, D Tchomakov, et al.
Annales De Genetique|February 16, 2000
Schinzel-Giedion syndrome with severe deafness and neurodegenerative processY Alembik, D Christmann, A de Saint Martin, et al.
American Journal of Medical Genetics. Part A|July 22, 2004
Turner syndrome: evaluation of prenatal diagnosis in 19 European registriesNeus Baena, C De Vigan, E Cariati, et al.
Journal of Cancer Research and Clinical Oncology|August 3, 2014
Discontinuation and non-adherence to endocrine therapy in breast cancer patients: is lack of communication the decisive factor?P Wuensch, A Hahne, R Haidinger, et al.
European Journal of Clinical Pharmacology|January 1, 1989
Acetylator phenotype and congenital malformationsC Stoll, M P Roth, B Dott, et al.
Annales De Genetique|December 8, 2004
Contribution of ultrasonographic examination to the prenatal detection of trisomy 21: experience from 19 European registersD Wellesley, C De Vigan, N Baena, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1982
[Auer bodies and Ph1 chromosome: chronic myeloid pseudoleukemia?]S Mayer, A Falkenrodt, A Albert, et al.
Pageof 38

Showing results (291-300 of 377) with videos related to

Sort By:
Pageof 38
American Journal of Medical Genetics. Part A|April 11, 2003
Prenatal detection of rare chromosomal autosomal abnormalities in EuropeN Baena, C De Vigan, E Cariati, et al.
Intensive Care Medicine|February 8, 2000
Effects of noninvasive positive pressure ventilatory support in non-COPD patients with acute respiratory insufficiency after early extubationE Kilger, J Briegel, M Haller, et al.
Annales De Genetique|January 1, 1996
A study on limb reduction defects in six European regionsC Stoll, E Calzolari, M Cornel, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Severe hypernatremic dehydration in an infant with Netherton syndromeC Stoll, Y Alembik, D Tchomakov, et al.
Annales De Genetique|February 16, 2000
Schinzel-Giedion syndrome with severe deafness and neurodegenerative processY Alembik, D Christmann, A de Saint Martin, et al.
American Journal of Medical Genetics. Part A|July 22, 2004
Turner syndrome: evaluation of prenatal diagnosis in 19 European registriesNeus Baena, C De Vigan, E Cariati, et al.
Journal of Cancer Research and Clinical Oncology|August 3, 2014
Discontinuation and non-adherence to endocrine therapy in breast cancer patients: is lack of communication the decisive factor?P Wuensch, A Hahne, R Haidinger, et al.
European Journal of Clinical Pharmacology|January 1, 1989
Acetylator phenotype and congenital malformationsC Stoll, M P Roth, B Dott, et al.
Annales De Genetique|December 8, 2004
Contribution of ultrasonographic examination to the prenatal detection of trisomy 21: experience from 19 European registersD Wellesley, C De Vigan, N Baena, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1982
[Auer bodies and Ph1 chromosome: chronic myeloid pseudoleukemia?]S Mayer, A Falkenrodt, A Albert, et al.
Pageof 38