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Ingo Kennerknecht

Showing results (21-30 of 32) with videos related to

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Frontiers in Behavioral Neuroscience|December 6, 2021
Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face AreaAlexa Haeger, Christophe Pouzat, Volker Luecken, et al.
Cancer Genetics and Cytogenetics|March 14, 2002
Novel der(1)t(1;19) in two patients with myeloid neoplasiasJoëlle Tchinda, Sarah Volpert, Thomas Neumann, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|August 23, 2007
Hereditary prosopagnosia: the first case seriesMartina Grueter, Thomas Grueter, Vaughan Bell, et al.
American Journal of Medical Genetics. Part A|November 10, 2004
Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studiesDaniela Ehling, Ingo Kennerknecht, Annelore Junge, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
Situs ambiguus in a female fetus with balanced (X;21) translocation--evidence for functional nullisomy of the ZIC3 gene?Barbara Fritz, Jürgen Kunz, Gun Peggy Strømstad Knudsen, et al.
Molecular Biology and Evolution|November 10, 2010
Unexpected island effects at an extreme: reduced Y chromosome and mitochondrial DNA diversity in NiasMannis van Oven, Johannes M Hämmerle, Marja van Schoor, et al.
Leukemia & Lymphoma|January 24, 2004
Multicolor karyotyping in acute myeloid leukemiaJoëlle Tchinda, Sarah Volpert, Nicole McNeil, et al.
Clinical Genetics|November 9, 2021
Expanding the spectrum of syndromic PPP2R3C-related XY gonadal dysgenesis to XX gonadal dysgenesisUmut Altunoglu, Esra Börklü, Anju Shukla, et al.
Human Genetics|April 21, 2015
Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3Birgit S Budde, Shuji Mizumoto, Ryo Kogawa, et al.
Nature Communications|July 7, 2016
MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfectaUschi Lindert, Wayne A Cabral, Surasawadee Ausavarat, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Frontiers in Behavioral Neuroscience|December 6, 2021
Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face AreaAlexa Haeger, Christophe Pouzat, Volker Luecken, et al.
Cancer Genetics and Cytogenetics|March 14, 2002
Novel der(1)t(1;19) in two patients with myeloid neoplasiasJoëlle Tchinda, Sarah Volpert, Thomas Neumann, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|August 23, 2007
Hereditary prosopagnosia: the first case seriesMartina Grueter, Thomas Grueter, Vaughan Bell, et al.
American Journal of Medical Genetics. Part A|November 10, 2004
Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studiesDaniela Ehling, Ingo Kennerknecht, Annelore Junge, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
Situs ambiguus in a female fetus with balanced (X;21) translocation--evidence for functional nullisomy of the ZIC3 gene?Barbara Fritz, Jürgen Kunz, Gun Peggy Strømstad Knudsen, et al.
Molecular Biology and Evolution|November 10, 2010
Unexpected island effects at an extreme: reduced Y chromosome and mitochondrial DNA diversity in NiasMannis van Oven, Johannes M Hämmerle, Marja van Schoor, et al.
Leukemia & Lymphoma|January 24, 2004
Multicolor karyotyping in acute myeloid leukemiaJoëlle Tchinda, Sarah Volpert, Nicole McNeil, et al.
Clinical Genetics|November 9, 2021
Expanding the spectrum of syndromic PPP2R3C-related XY gonadal dysgenesis to XX gonadal dysgenesisUmut Altunoglu, Esra Börklü, Anju Shukla, et al.
Human Genetics|April 21, 2015
Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3Birgit S Budde, Shuji Mizumoto, Ryo Kogawa, et al.
Nature Communications|July 7, 2016
MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfectaUschi Lindert, Wayne A Cabral, Surasawadee Ausavarat, et al.
Pageof 4