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Horsthemke

Showing results (231-240 of 368) with videos related to

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Journal of Medical Genetics|July 10, 2008
Biallelic loss of function of the promyelocytic leukaemia zinc finger (PLZF) gene causes severe skeletal defects and genital hypoplasiaS Fischer, J Kohlhase, D Böhm, et al.
American Journal of Medical Genetics|May 1, 1991
Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastomaK Kloss, P Währisch, V Greger, et al.
Human Genetics|November 1, 1992
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13B Dittrich, W P Robinson, H Knoblauch, et al.
Arteriosclerosis (Dallas, Tex.)|January 1, 1989
Gene probes in diagnosis of familial hypercholesterolemiaS Humphries, R Taylor, M Jeenah, et al.
Neurogenetics|December 19, 2009
The C15orf2 gene in the Prader-Willi syndrome region is subject to genomic imprinting and positive selectionMichaela Wawrzik, Unga Arifa Unmehopa, Dick Frans Swaab, et al.
European Journal of Human Genetics : EJHG|June 15, 2006
Syndrome identification based on 2D analysis softwareStefan Boehringer, Tobias Vollmar, Christiane Tasse, et al.
Orphanet Journal of Rare Diseases|March 26, 2014
Clinical phenotypes of MAGEL2 mutations and deletionsKarin Buiting, Nataliya Di Donato, Jasmin Beygo, et al.
Clinical Genetics|November 15, 2000
Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselingK Buiting, C Färber, P Kroisel, et al.
Human Molecular Genetics|September 24, 2004
Somatic mosaicism in patients with Angelman syndrome and an imprinting defectHülya Nazlican, Michael Zeschnigk, Uwe Claussen, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 1991
Long-term treatment effects in patients with bilateral retinoblastoma: ocular and mid-facial findingsE P Messmer, H Fritze, C Mohr, et al.
Pageof 37

Showing results (231-240 of 368) with videos related to

Sort By:
Pageof 37
Journal of Medical Genetics|July 10, 2008
Biallelic loss of function of the promyelocytic leukaemia zinc finger (PLZF) gene causes severe skeletal defects and genital hypoplasiaS Fischer, J Kohlhase, D Böhm, et al.
American Journal of Medical Genetics|May 1, 1991
Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastomaK Kloss, P Währisch, V Greger, et al.
Human Genetics|November 1, 1992
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13B Dittrich, W P Robinson, H Knoblauch, et al.
Arteriosclerosis (Dallas, Tex.)|January 1, 1989
Gene probes in diagnosis of familial hypercholesterolemiaS Humphries, R Taylor, M Jeenah, et al.
Neurogenetics|December 19, 2009
The C15orf2 gene in the Prader-Willi syndrome region is subject to genomic imprinting and positive selectionMichaela Wawrzik, Unga Arifa Unmehopa, Dick Frans Swaab, et al.
European Journal of Human Genetics : EJHG|June 15, 2006
Syndrome identification based on 2D analysis softwareStefan Boehringer, Tobias Vollmar, Christiane Tasse, et al.
Orphanet Journal of Rare Diseases|March 26, 2014
Clinical phenotypes of MAGEL2 mutations and deletionsKarin Buiting, Nataliya Di Donato, Jasmin Beygo, et al.
Clinical Genetics|November 15, 2000
Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselingK Buiting, C Färber, P Kroisel, et al.
Human Molecular Genetics|September 24, 2004
Somatic mosaicism in patients with Angelman syndrome and an imprinting defectHülya Nazlican, Michael Zeschnigk, Uwe Claussen, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 1991
Long-term treatment effects in patients with bilateral retinoblastoma: ocular and mid-facial findingsE P Messmer, H Fritze, C Mohr, et al.
Pageof 37