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Pathology, Research and Practice
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October 24, 2022
Fatal course of a benign mediastinal lipoblastoma in a 20-year-old woman
Christine Ganzert, Anton Popov, Eva Lücke, et al.
International Journal of Molecular Sciences
|
February 15, 2022
Profiling of the Bacterial Microbiota along the Murine Alimentary Tract
Ramiro Vilchez-Vargas, Franz Salm, Eva B Znalesniak, et al.
Scientific Reports
|
June 25, 2026
Systematic assessment for potential endogenous normalizers for microRNA analysis in fecal samples
Theresa Lederer, Konrad Lehr, Cosima Thon, et al.
Clinical Dysmorphology
|
December 24, 2011
A patient with a skull defect, dysmorphic features, hypopituitarism, and abnormal cortical development
Patrizia Accorsi, Lucio Giordano, Vera Uliana, et al.
American Journal of Medical Genetics. Part A
|
November 14, 2008
Johanson-Blizzard syndrome caused by identical UBR1 mutations in two unrelated girls, one with a cardiomyopathy
Mariet Elting, Ariana Kariminejad, Marie-Louise de Sonnaville, et al.
Cancer Gene Therapy
|
February 15, 2024
Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice
Miriam Mengoni, Andreas Dominik Braun, Sahithi Seedarala, et al.
Cellular and Molecular Neurobiology
|
November 21, 2024
Rasopathy-Associated Mutation Ptpn11<sup>D61Y</sup> has Age-Dependent Effect on Synaptic Vesicle Recycling
Debarpan Guhathakurta, Franziska Selzam, Aneta Petrušková, et al.
American Journal of Medical Genetics. Part A
|
September 18, 2009
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome
John M Graham, Nancy Kramer, Bassem A Bejjani, et al.
American Journal of Medical Genetics. Part A
|
July 18, 2009
The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects
Katie M G Snape, Deborah Ruddy, Martin Zenker, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 19, 2015
Remission of congenital hyperinsulinism following conservative treatment: an exploratory study in patients with KATP channel mutations
Mark J Lachmann, Burak Salgin, Sebastian Kummer, et al.
Page
of 34
Search research articles
Search
Showing results (111-120 of 338) with videos related to
Sort By:
Page
of 34
Pathology, Research and Practice
|
October 24, 2022
Fatal course of a benign mediastinal lipoblastoma in a 20-year-old woman
Christine Ganzert, Anton Popov, Eva Lücke, et al.
International Journal of Molecular Sciences
|
February 15, 2022
Profiling of the Bacterial Microbiota along the Murine Alimentary Tract
Ramiro Vilchez-Vargas, Franz Salm, Eva B Znalesniak, et al.
Scientific Reports
|
June 25, 2026
Systematic assessment for potential endogenous normalizers for microRNA analysis in fecal samples
Theresa Lederer, Konrad Lehr, Cosima Thon, et al.
Clinical Dysmorphology
|
December 24, 2011
A patient with a skull defect, dysmorphic features, hypopituitarism, and abnormal cortical development
Patrizia Accorsi, Lucio Giordano, Vera Uliana, et al.
American Journal of Medical Genetics. Part A
|
November 14, 2008
Johanson-Blizzard syndrome caused by identical UBR1 mutations in two unrelated girls, one with a cardiomyopathy
Mariet Elting, Ariana Kariminejad, Marie-Louise de Sonnaville, et al.
Cancer Gene Therapy
|
February 15, 2024
Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice
Miriam Mengoni, Andreas Dominik Braun, Sahithi Seedarala, et al.
Cellular and Molecular Neurobiology
|
November 21, 2024
Rasopathy-Associated Mutation Ptpn11<sup>D61Y</sup> has Age-Dependent Effect on Synaptic Vesicle Recycling
Debarpan Guhathakurta, Franziska Selzam, Aneta Petrušková, et al.
American Journal of Medical Genetics. Part A
|
September 18, 2009
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome
John M Graham, Nancy Kramer, Bassem A Bejjani, et al.
American Journal of Medical Genetics. Part A
|
July 18, 2009
The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects
Katie M G Snape, Deborah Ruddy, Martin Zenker, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 19, 2015
Remission of congenital hyperinsulinism following conservative treatment: an exploratory study in patients with KATP channel mutations
Mark J Lachmann, Burak Salgin, Sebastian Kummer, et al.
Page
of 34