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Klinische Padiatrie
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September 15, 2022
Impact of the COVID-19 Pandemic Regulations on the Health Status and Medical Care of Children with Trisomy 21
Annika Niemann, Anett Boudriot, Birgit Brett, et al.
American Journal of Medical Genetics. Part A
|
June 4, 2020
Characteristic dental pattern with hypodontia and short roots in Fraser syndrome
Felix Kunz, Hülya Kayserili, Alina Midro, et al.
Frontiers in Psychology
|
May 17, 2017
Behavioral and Neural Manifestations of Reward Memory in Carriers of Low-Expressing versus High-Expressing Genetic Variants of the Dopamine D2 Receptor
Anni Richter, Adriana Barman, Torsten Wüstenberg, et al.
The EMBO Journal
|
February 6, 2015
Synaptic activity controls localization and function of CtBP1 via binding to Bassoon and Piccolo
Daniela Ivanova, Anika Dirks, Carolina Montenegro-Venegas, et al.
Frontiers in Immunology
|
August 19, 2022
T cell-specific constitutive active SHP2 enhances T cell memory formation and reduces T cell activation
Clemens Cammann, Nicole Israel, Sarah Frentzel, et al.
American Journal of Medical Genetics. Part A
|
August 19, 2006
Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation
Anita Rauch, Juliane Hoyer, Sabine Guth, et al.
The Journal of Pediatrics
|
March 6, 2004
Genotype-phenotype correlations in Noonan syndrome
Martin Zenker, Gernot Buheitel, Ralf Rauch, et al.
Journal of the Endocrine Society
|
April 27, 2022
Correlation of PET-MRI, Pathology, LOH, and Surgical Success in a Case of CHI With Atypical Large Pancreatic Focus
Hendrik Vossschulte, Konrad Mohnike, Klaus Mohnike, et al.
Gut
|
June 11, 2015
ABO blood type B and fucosyltransferase 2 non-secretor status as genetic risk factors for chronic pancreatitis
Frank Ulrich Weiss, Claudia Schurmann, Alexander Teumer, et al.
European Journal of Medical Genetics
|
November 10, 2021
European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe
Sixto García-Miñaúr, Emma Burkitt-Wright, Alain Verloes, et al.
Page
of 34
Search research articles
Search
Showing results (161-170 of 338) with videos related to
Sort By:
Page
of 34
Klinische Padiatrie
|
September 15, 2022
Impact of the COVID-19 Pandemic Regulations on the Health Status and Medical Care of Children with Trisomy 21
Annika Niemann, Anett Boudriot, Birgit Brett, et al.
American Journal of Medical Genetics. Part A
|
June 4, 2020
Characteristic dental pattern with hypodontia and short roots in Fraser syndrome
Felix Kunz, Hülya Kayserili, Alina Midro, et al.
Frontiers in Psychology
|
May 17, 2017
Behavioral and Neural Manifestations of Reward Memory in Carriers of Low-Expressing versus High-Expressing Genetic Variants of the Dopamine D2 Receptor
Anni Richter, Adriana Barman, Torsten Wüstenberg, et al.
The EMBO Journal
|
February 6, 2015
Synaptic activity controls localization and function of CtBP1 via binding to Bassoon and Piccolo
Daniela Ivanova, Anika Dirks, Carolina Montenegro-Venegas, et al.
Frontiers in Immunology
|
August 19, 2022
T cell-specific constitutive active SHP2 enhances T cell memory formation and reduces T cell activation
Clemens Cammann, Nicole Israel, Sarah Frentzel, et al.
American Journal of Medical Genetics. Part A
|
August 19, 2006
Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation
Anita Rauch, Juliane Hoyer, Sabine Guth, et al.
The Journal of Pediatrics
|
March 6, 2004
Genotype-phenotype correlations in Noonan syndrome
Martin Zenker, Gernot Buheitel, Ralf Rauch, et al.
Journal of the Endocrine Society
|
April 27, 2022
Correlation of PET-MRI, Pathology, LOH, and Surgical Success in a Case of CHI With Atypical Large Pancreatic Focus
Hendrik Vossschulte, Konrad Mohnike, Klaus Mohnike, et al.
Gut
|
June 11, 2015
ABO blood type B and fucosyltransferase 2 non-secretor status as genetic risk factors for chronic pancreatitis
Frank Ulrich Weiss, Claudia Schurmann, Alexander Teumer, et al.
European Journal of Medical Genetics
|
November 10, 2021
European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe
Sixto García-Miñaúr, Emma Burkitt-Wright, Alain Verloes, et al.
Page
of 34