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C Hilger

Showing results (41-50 of 93) with videos related to

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Asia Pacific Journal of Clinical Nutrition|December 10, 2017
Low maternal folate concentrations and maternal MTHFR C677T polymorphism are associated with an increased risk for neural tube defects in offspring: a case-control study among Pakistani case and control mothersNuzhat Nauman, Samina Jalali, Sajjad Shami, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|December 19, 2015
Whole-Exome Sequencing in Nine Monozygotic Discordant TwinsRong Zhang, Holger Thiele, Peter Bartmann, et al.
Allergy|April 26, 2017
Identification of a polygalacturonase (Cup s 2) as the major CCD-bearing allergen in Cupressus sempervirens pollenY Shahali, J-P Sutra, C Hilger, et al.
American Journal of Medical Genetics|June 5, 1998
Association between novelty-seeking and the dopamine D3 receptor gene in bipolar patients: a preliminary reportL Staner, C Hilger, F Hentges, et al.
Lower Urinary Tract Symptoms|April 18, 2018
A classic twin study of lower urinary tract obstruction: Report of 3 cases and literature reviewSandra Frese, Alexander Weigert, Bernd Hoppe, et al.
The Journal of Clinical Endocrinology and Metabolism|January 9, 2016
Infancy-Onset T1DM, Short Stature, and Severe Immunodysregulation in Two Siblings With a Homozygous LRBA MutationFelix Schreiner, Michaela Plamper, Gesche Dueker, et al.
Molecular Medicine Reports|March 18, 2015
Mutations in PTF1A are not a common cause for human VATER/VACTERL association or neural tube defects mirroring Danforth's short tail mouseNirmala Gurung, Greta Grosse, Markus Draaken, et al.
Journal of Neurodevelopmental Disorders|April 19, 2016
Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVsMadita Schumann, Andrea Hofmann, Sophia K Krutzke, et al.
Birth Defects Research|March 20, 2019
HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrumFranziska Kause, Rong Zhang, Michael Ludwig, et al.
American Journal of Medical Genetics|July 18, 2000
5-HT2a receptor polymorphism gene in bipolar disorder and harm avoidance personality traitS Blairy, I Massat, L Staner, et al.
Pageof 10

Showing results (41-50 of 93) with videos related to

Sort By:
Pageof 10
Asia Pacific Journal of Clinical Nutrition|December 10, 2017
Low maternal folate concentrations and maternal MTHFR C677T polymorphism are associated with an increased risk for neural tube defects in offspring: a case-control study among Pakistani case and control mothersNuzhat Nauman, Samina Jalali, Sajjad Shami, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|December 19, 2015
Whole-Exome Sequencing in Nine Monozygotic Discordant TwinsRong Zhang, Holger Thiele, Peter Bartmann, et al.
Allergy|April 26, 2017
Identification of a polygalacturonase (Cup s 2) as the major CCD-bearing allergen in Cupressus sempervirens pollenY Shahali, J-P Sutra, C Hilger, et al.
American Journal of Medical Genetics|June 5, 1998
Association between novelty-seeking and the dopamine D3 receptor gene in bipolar patients: a preliminary reportL Staner, C Hilger, F Hentges, et al.
Lower Urinary Tract Symptoms|April 18, 2018
A classic twin study of lower urinary tract obstruction: Report of 3 cases and literature reviewSandra Frese, Alexander Weigert, Bernd Hoppe, et al.
The Journal of Clinical Endocrinology and Metabolism|January 9, 2016
Infancy-Onset T1DM, Short Stature, and Severe Immunodysregulation in Two Siblings With a Homozygous LRBA MutationFelix Schreiner, Michaela Plamper, Gesche Dueker, et al.
Molecular Medicine Reports|March 18, 2015
Mutations in PTF1A are not a common cause for human VATER/VACTERL association or neural tube defects mirroring Danforth's short tail mouseNirmala Gurung, Greta Grosse, Markus Draaken, et al.
Journal of Neurodevelopmental Disorders|April 19, 2016
Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVsMadita Schumann, Andrea Hofmann, Sophia K Krutzke, et al.
Birth Defects Research|March 20, 2019
HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrumFranziska Kause, Rong Zhang, Michael Ludwig, et al.
American Journal of Medical Genetics|July 18, 2000
5-HT2a receptor polymorphism gene in bipolar disorder and harm avoidance personality traitS Blairy, I Massat, L Staner, et al.
Pageof 10