Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Heiko Reutter

Showing results (91-100 of 209) with videos related to

Pageof 21
Sort By:
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.
Children (Basel, Switzerland)|January 23, 2024
Diagnostic Utility of Interleukin-6 in Early-Onset Sepsis among Term Newborns: Impact of Maternal Risk Factors and CRP EvaluationMaria Schleier, Julia Lubig, Sven Kehl, et al.
American Journal of Medical Genetics. Part A|February 6, 2008
Mutation screening in the IRF6-gene in patients with apparently nonsyndromic orofacial clefts and a positive family history suggestive of autosomal-dominant inheritanceStefanie Birnbaum, Heiko Reutter, Carola Lauster, et al.
Clinical Case Reports|September 15, 2018
Congenital diaphragmatic hernia in a case of Cat eye syndromeEbru Aileen Alsat, Heiko Reutter, Soyhan Bagci, et al.
International Journal of Molecular Medicine|November 3, 2010
p63 (TP73L) a key player in embryonic urogenital development with significant dysregulation in human bladder exstrophy tissueBonnie J Ching, Lars Wittler, Judith Proske, 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.
Gene|July 7, 2012
Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadiasLars Wittler, Alina Hilger, Judith Proske, et al.
Pageof 21

Showing results (91-100 of 209) with videos related to

Sort By:
Pageof 21
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.
Children (Basel, Switzerland)|January 23, 2024
Diagnostic Utility of Interleukin-6 in Early-Onset Sepsis among Term Newborns: Impact of Maternal Risk Factors and CRP EvaluationMaria Schleier, Julia Lubig, Sven Kehl, et al.
American Journal of Medical Genetics. Part A|February 6, 2008
Mutation screening in the IRF6-gene in patients with apparently nonsyndromic orofacial clefts and a positive family history suggestive of autosomal-dominant inheritanceStefanie Birnbaum, Heiko Reutter, Carola Lauster, et al.
Clinical Case Reports|September 15, 2018
Congenital diaphragmatic hernia in a case of Cat eye syndromeEbru Aileen Alsat, Heiko Reutter, Soyhan Bagci, et al.
International Journal of Molecular Medicine|November 3, 2010
p63 (TP73L) a key player in embryonic urogenital development with significant dysregulation in human bladder exstrophy tissueBonnie J Ching, Lars Wittler, Judith Proske, 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.
Gene|July 7, 2012
Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadiasLars Wittler, Alina Hilger, Judith Proske, et al.
Pageof 21