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E Klopocki

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

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Journal of Medical Genetics|January 8, 2008
A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndromeE Klopocki, C-E Ott, N Benatar, et al.
Clinical Genetics|July 12, 2008
Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4E Steichen-Gersdorf, I Gassner, A Superti-Furga, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|November 27, 2007
[Epigenetic inactivation of the WNT antagonist SFRP1 in breast cancer]E Dahl, J Veeck, H An, et al.
Clinical Genetics|February 22, 2013
Novel mutations of the PRKAR1A gene in patients with acrodysostosisF Muhn, E Klopocki, L Graul-Neumann, et al.
Clinical Genetics|May 27, 2015
DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnosticsB Vona, M A H Hofrichter, C Neuner, et al.
Oncogene|February 2, 2006
Aberrant methylation of the Wnt antagonist SFRP1 in breast cancer is associated with unfavourable prognosisJ Veeck, D Niederacher, H An, et al.
Oncogene|March 14, 2007
Frequent loss of SFRP1 expression in multiple human solid tumours: association with aberrant promoter methylation in renal cell carcinomaE Dahl, F Wiesmann, M Woenckhaus, et al.
Clinical Genetics|January 25, 2014
Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndromeS Lohan, M Spielmann, S C Doelken, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
Pageof 1

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

Sort By:
Pageof 1
Journal of Medical Genetics|January 8, 2008
A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndromeE Klopocki, C-E Ott, N Benatar, et al.
Clinical Genetics|July 12, 2008
Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4E Steichen-Gersdorf, I Gassner, A Superti-Furga, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|November 27, 2007
[Epigenetic inactivation of the WNT antagonist SFRP1 in breast cancer]E Dahl, J Veeck, H An, et al.
Clinical Genetics|February 22, 2013
Novel mutations of the PRKAR1A gene in patients with acrodysostosisF Muhn, E Klopocki, L Graul-Neumann, et al.
Clinical Genetics|May 27, 2015
DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnosticsB Vona, M A H Hofrichter, C Neuner, et al.
Oncogene|February 2, 2006
Aberrant methylation of the Wnt antagonist SFRP1 in breast cancer is associated with unfavourable prognosisJ Veeck, D Niederacher, H An, et al.
Oncogene|March 14, 2007
Frequent loss of SFRP1 expression in multiple human solid tumours: association with aberrant promoter methylation in renal cell carcinomaE Dahl, F Wiesmann, M Woenckhaus, et al.
Clinical Genetics|January 25, 2014
Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndromeS Lohan, M Spielmann, S C Doelken, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
Pageof 1