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J Müsebeck

Showing results (1-10 of 7) with videos related to

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The British Journal of Dermatology|May 28, 2008
Somatic FGFR3 and PIK3CA mutations are present in familial seborrhoeic keratosesC Hafner, T Vogt, M Landthaler, et al.
Journal of Thrombosis and Haemostasis : JTH|March 24, 2009
Molecular mechanisms underlying hemophilia A phenotype in seven femalesA Pavlova, H Brondke, J Müsebeck, et al.
Journal of Medical Genetics|February 12, 2002
Partial trisomy 9p12p21.3 with a normal phenotypeM Stumm, J Müsebeck, H Tönnies, et al.
Journal of Medical Genetics|June 5, 2001
Two further cases of WHS with unbalanced de novo translocation t(4;8) characterised by CGH and FISHH Tönnies, M Stumm, L Neumann, et al.
Human Reproduction (Oxford, England)|July 13, 1999
Frequency of CFTR gene mutations in males participating in an ICSI programmeS Jakubiczka, T Bettecken, M Stumm, et al.
Clinical Genetics|July 16, 2003
Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphismT Liehr, M Ziegler, H Starke, et al.
Journal of Medical Genetics|April 7, 2009
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and functionF Lacbawan, B D Solomon, E Roessler, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
The British Journal of Dermatology|May 28, 2008
Somatic FGFR3 and PIK3CA mutations are present in familial seborrhoeic keratosesC Hafner, T Vogt, M Landthaler, et al.
Journal of Thrombosis and Haemostasis : JTH|March 24, 2009
Molecular mechanisms underlying hemophilia A phenotype in seven femalesA Pavlova, H Brondke, J Müsebeck, et al.
Journal of Medical Genetics|February 12, 2002
Partial trisomy 9p12p21.3 with a normal phenotypeM Stumm, J Müsebeck, H Tönnies, et al.
Journal of Medical Genetics|June 5, 2001
Two further cases of WHS with unbalanced de novo translocation t(4;8) characterised by CGH and FISHH Tönnies, M Stumm, L Neumann, et al.
Human Reproduction (Oxford, England)|July 13, 1999
Frequency of CFTR gene mutations in males participating in an ICSI programmeS Jakubiczka, T Bettecken, M Stumm, et al.
Clinical Genetics|July 16, 2003
Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphismT Liehr, M Ziegler, H Starke, et al.
Journal of Medical Genetics|April 7, 2009
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and functionF Lacbawan, B D Solomon, E Roessler, et al.
Pageof 1