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Michael Ludwig

Showing results (151-160 of 239) with videos related to

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Journal of Assisted Reproduction and Genetics|October 5, 2006
Distribution of persistent organochlorine contaminants in infertile patients from Tanzania and GermanyJürgen M Weiss, Otmar Bauer, Albrecht Blüthgen, 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.
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.
European Journal of Medical Genetics|September 21, 2010
De novo microduplication at 22q11.21 in a patient with VACTERL associationCharlotte Schramm, Markus Draaken, Enrika Bartels, et al.
Diagnostics (Basel, Switzerland)|December 22, 2023
Prospective Comparison of Handheld Ultrasound Devices from Different Manufacturers with Respect to B-Scan Quality and Clinical Significance for Various Abdominal Sonography QuestionsDaniel Merkel, Tim Felix Züllich, Christoph Schneider, et al.
Pediatric Surgery International|March 17, 2012
Familial occurrence of the VATER/VACTERL associationAlina Hilger, Charlotte Schramm, Markus Draaken, 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.
Frontiers in Bioscience (Landmark Edition)|June 24, 2022
Mannose-Binding Lectin (MBL) and Gap Junction Protein Alpha 4 (GJA4) Gene Heterogeneity in Relation to Severity of Clinical Disease in Cystic FibrosisJoern Pascal Laubach, Michael Ludwig, Tabea Horn, et al.
Human Genetics|January 13, 2011
Maternal de novo triple mosaicism for two single OCRL nucleotide substitutions (c.1736A>T, c.1736A>G) in a Lowe syndrome familyMarkus Draaken, Carmen A Giesen, Anne L Kesselheim, et al.
Epilepsy Research|May 14, 2003
Allopregnanolone serum levels and expression of 5 alpha-reductase and 3 alpha-hydroxysteroid dehydrogenase isoforms in hippocampal and temporal cortex of patients with epilepsyBirgit Stoffel-Wagner, Matthias Watzka, Stephan Steckelbroeck, et al.
Pageof 24

Showing results (151-160 of 239) with videos related to

Sort By:
Pageof 24
Journal of Assisted Reproduction and Genetics|October 5, 2006
Distribution of persistent organochlorine contaminants in infertile patients from Tanzania and GermanyJürgen M Weiss, Otmar Bauer, Albrecht Blüthgen, 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.
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.
European Journal of Medical Genetics|September 21, 2010
De novo microduplication at 22q11.21 in a patient with VACTERL associationCharlotte Schramm, Markus Draaken, Enrika Bartels, et al.
Diagnostics (Basel, Switzerland)|December 22, 2023
Prospective Comparison of Handheld Ultrasound Devices from Different Manufacturers with Respect to B-Scan Quality and Clinical Significance for Various Abdominal Sonography QuestionsDaniel Merkel, Tim Felix Züllich, Christoph Schneider, et al.
Pediatric Surgery International|March 17, 2012
Familial occurrence of the VATER/VACTERL associationAlina Hilger, Charlotte Schramm, Markus Draaken, 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.
Frontiers in Bioscience (Landmark Edition)|June 24, 2022
Mannose-Binding Lectin (MBL) and Gap Junction Protein Alpha 4 (GJA4) Gene Heterogeneity in Relation to Severity of Clinical Disease in Cystic FibrosisJoern Pascal Laubach, Michael Ludwig, Tabea Horn, et al.
Human Genetics|January 13, 2011
Maternal de novo triple mosaicism for two single OCRL nucleotide substitutions (c.1736A>T, c.1736A>G) in a Lowe syndrome familyMarkus Draaken, Carmen A Giesen, Anne L Kesselheim, et al.
Epilepsy Research|May 14, 2003
Allopregnanolone serum levels and expression of 5 alpha-reductase and 3 alpha-hydroxysteroid dehydrogenase isoforms in hippocampal and temporal cortex of patients with epilepsyBirgit Stoffel-Wagner, Matthias Watzka, Stephan Steckelbroeck, et al.
Pageof 24