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F Fellmann

Showing results (1-10 of 22) with videos related to

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Revue Medicale Suisse|July 10, 2008
[Genetic dermatology clinics: a practical approach]D Hohl, F Fellmann
Biotechniques|November 1, 1996
Simplified protocol of solid-phase cDNA libraries for multiple PCR amplificationF Fellmann, J L Pretet, D Fellmann
Cytogenetics and Cell Genetics|April 18, 2001
Meiotic segregation analysis by FISH investigation of spermatozoa of a 46,Y,der(X),t(X;Y)(qter-->p22::q11-->qter) carrierF Morel, F Fellmann, C Roux, et al.
Prenatal Diagnosis|November 1, 1996
Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q)S Mercier, F Fellmann, J Cattin, et al.
Clinical Genetics|October 30, 2009
Sudden death: ethical and legal problems of post-mortem forensic genetic testing for hereditary cardiac diseasesB S Elger, K Michaud, F Fellmann, et al.
Molecular Human Reproduction|August 24, 2000
AZFa deletions in Sertoli cell-only syndrome: a retrospective studyO Blagosklonova, F Fellmann, M C Clavequin, et al.
European Journal of Neurology|May 22, 2009
Bilateral carotid thrombus formation after strenuous coughingF Siclari, L Hirt, R Meuli, et al.
Human Mutation|April 19, 2006
Confirmation of the origin of NISCH syndromeL Feldmeyer, M Huber, F Fellmann, et al.
Joint Bone Spine|April 28, 2001
Adult hypophosphatasia. Current aspectsD Wendling, L Jeannin-Louys, P Kremer, et al.
Human Reproduction (Oxford, England)|August 2, 2002
Absence of anti-Müllerian hormone (AMH) and M2A immunoreactivities in Sertoli cell-only syndrome and maturation arrest with and without AZF microdeletionsO Blagosklonova, C Joanne, C Roux, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Revue Medicale Suisse|July 10, 2008
[Genetic dermatology clinics: a practical approach]D Hohl, F Fellmann
Biotechniques|November 1, 1996
Simplified protocol of solid-phase cDNA libraries for multiple PCR amplificationF Fellmann, J L Pretet, D Fellmann
Cytogenetics and Cell Genetics|April 18, 2001
Meiotic segregation analysis by FISH investigation of spermatozoa of a 46,Y,der(X),t(X;Y)(qter-->p22::q11-->qter) carrierF Morel, F Fellmann, C Roux, et al.
Prenatal Diagnosis|November 1, 1996
Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q)S Mercier, F Fellmann, J Cattin, et al.
Clinical Genetics|October 30, 2009
Sudden death: ethical and legal problems of post-mortem forensic genetic testing for hereditary cardiac diseasesB S Elger, K Michaud, F Fellmann, et al.
Molecular Human Reproduction|August 24, 2000
AZFa deletions in Sertoli cell-only syndrome: a retrospective studyO Blagosklonova, F Fellmann, M C Clavequin, et al.
European Journal of Neurology|May 22, 2009
Bilateral carotid thrombus formation after strenuous coughingF Siclari, L Hirt, R Meuli, et al.
Human Mutation|April 19, 2006
Confirmation of the origin of NISCH syndromeL Feldmeyer, M Huber, F Fellmann, et al.
Joint Bone Spine|April 28, 2001
Adult hypophosphatasia. Current aspectsD Wendling, L Jeannin-Louys, P Kremer, et al.
Human Reproduction (Oxford, England)|August 2, 2002
Absence of anti-Müllerian hormone (AMH) and M2A immunoreactivities in Sertoli cell-only syndrome and maturation arrest with and without AZF microdeletionsO Blagosklonova, C Joanne, C Roux, et al.
Pageof 3