Search research articles
Contact Us
Filters
Showing results (21-30 of 42) with videos related to
Page
of 5
Sort By:
Plos One
|
February 10, 2011
MicroRNAs differentially expressed in postnatal aortic development downregulate elastin via 3' UTR and coding-sequence binding sites
Claus Eric Ott, Johannes Grünhagen, Marten Jäger, et al.
Frontiers in Neuroscience
|
December 26, 2024
Impact of genetic test interpretation on a <i>VPS13B</i> missense variant in Cohen syndrome
Gudrun Schottmann, Carmen Martínez Almudéver, Julia C M Knop, et al.
JBMR Plus
|
October 5, 2018
The Interaction of BMP2-Induced Defect Healing in Rat and Fixator Stiffness Modulates Matrix Alignment and Contraction
Carolin Schwarz, Claus-Eric Ott, Dag Wulsten, et al.
Molecular Genetics and Metabolism
|
June 11, 2014
Severe congenital cutis laxa with cardiovascular manifestations due to homozygous deletions in ALDH18A1
Björn Fischer, Bert Callewaert, Phillipe Schröter, et al.
Journal of Medical Internet Research
|
October 22, 2020
Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study
Jean Tori Pantel, Nurulhuda Hajjir, Magdalena Danyel, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2018
A novel mutation in CDH11, encoding cadherin-11, cause Branchioskeletogenital (Elsahy-Waters) syndrome
Marco Castori, Claus-Eric Ott, Luigi Bisceglia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 10, 2023
HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families
Annika Gottschalk, Henrike L Sczakiel, Wiebke Hülsemann, et al.
Bone
|
December 28, 2014
Improved bone defect healing by a superagonistic GDF5 variant derived from a patient with multiple synostoses syndrome
Elisa Degenkolbe, Carolin Schwarz, Claus-Eric Ott, et al.
Journal of Cardiovascular Electrophysiology
|
March 17, 2020
Novel variants in TECRL cause recessive inherited CPVT type 3 with severe and variable clinical symptoms
Alexander Moscu-Gregor, Christoph Marschall, Carsten Müntjes, et al.
Plos One
|
March 17, 2015
Double NF1 inactivation affects adrenocortical function in NF1Prx1 mice and a human patient
Karolina Kobus, Daniela Hartl, Claus Eric Ott, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 42) with videos related to
Sort By:
Page
of 5
Plos One
|
February 10, 2011
MicroRNAs differentially expressed in postnatal aortic development downregulate elastin via 3' UTR and coding-sequence binding sites
Claus Eric Ott, Johannes Grünhagen, Marten Jäger, et al.
Frontiers in Neuroscience
|
December 26, 2024
Impact of genetic test interpretation on a <i>VPS13B</i> missense variant in Cohen syndrome
Gudrun Schottmann, Carmen Martínez Almudéver, Julia C M Knop, et al.
JBMR Plus
|
October 5, 2018
The Interaction of BMP2-Induced Defect Healing in Rat and Fixator Stiffness Modulates Matrix Alignment and Contraction
Carolin Schwarz, Claus-Eric Ott, Dag Wulsten, et al.
Molecular Genetics and Metabolism
|
June 11, 2014
Severe congenital cutis laxa with cardiovascular manifestations due to homozygous deletions in ALDH18A1
Björn Fischer, Bert Callewaert, Phillipe Schröter, et al.
Journal of Medical Internet Research
|
October 22, 2020
Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study
Jean Tori Pantel, Nurulhuda Hajjir, Magdalena Danyel, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2018
A novel mutation in CDH11, encoding cadherin-11, cause Branchioskeletogenital (Elsahy-Waters) syndrome
Marco Castori, Claus-Eric Ott, Luigi Bisceglia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 10, 2023
HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families
Annika Gottschalk, Henrike L Sczakiel, Wiebke Hülsemann, et al.
Bone
|
December 28, 2014
Improved bone defect healing by a superagonistic GDF5 variant derived from a patient with multiple synostoses syndrome
Elisa Degenkolbe, Carolin Schwarz, Claus-Eric Ott, et al.
Journal of Cardiovascular Electrophysiology
|
March 17, 2020
Novel variants in TECRL cause recessive inherited CPVT type 3 with severe and variable clinical symptoms
Alexander Moscu-Gregor, Christoph Marschall, Carsten Müntjes, et al.
Plos One
|
March 17, 2015
Double NF1 inactivation affects adrenocortical function in NF1Prx1 mice and a human patient
Karolina Kobus, Daniela Hartl, Claus Eric Ott, et al.
Page
of 5