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Movement Disorders Clinical Practice
|
September 13, 2021
Commentary: Galactosemia Diagnosis by Whole Exome Sequencing Later in Life
Jennifer Friedman, Sara Lucas-Del-Pozo, David Moreno-Martinez, et al.
The American Journal of Pathology
|
October 5, 2010
Sera from preeclampsia patients elicit symptoms of human disease in mice and provide a basis for an in vitro predictive assay
Satyan Kalkunte, Roland Boij, Wendy Norris, et al.
Clinical Genetics
|
October 5, 2024
Consolidating the Role of Mutated ATP2B2 in Neurodevelopmental and Cerebellar Pathologies
Antonia M Stehr, Jerica Lenberg, Jennifer Friedman, et al.
Culture, Health & Sexuality
|
April 26, 2019
Experiences with abortion counselling in Mexico City and Colombia: addressing women's fears and concerns
Brianna Keefe-Oates, Shelly Makleff, Eleuthera Sa, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
November 27, 2014
Assessment of safety in newborns of mothers participating in clinical trials of vaccines administered during pregnancy
Flor M Munoz, Leonard E Weisman, Jennifer S Read, et al.
HGG Advances
|
October 27, 2025
Splicing and frameshift variants in QSER1 may be involved in developmental phenotypes
Megan C Fischer, Linda M Reis, Jerica Lenberg, et al.
Nature Chemical Biology
|
December 21, 2021
Characterization of a patient-derived variant of GPX4 for precision therapy
Hengrui Liu, Farhad Forouhar, Tobias Seibt, et al.
Human Molecular Genetics
|
October 8, 2021
Caenorhabditis elegans provides an efficient drug screening platform for GNAO1-related disorders and highlights the potential role of caffeine in controlling dyskinesia
Martina Di Rocco, Serena Galosi, Enrico Lanza, et al.
Pediatric Neurology
|
October 18, 2024
The Face and Features of RNU4-2: A New, Common, Recognizable, Yet Hidden Neurodevelopmental Disorder
Kristen Barbour, Matthew N Bainbridge, Kristen Wigby, et al.
Molecular Genetics & Genomic Medicine
|
June 2, 2021
Ending a diagnostic odyssey: Moving from exome to genome to identify cockayne syndrome
Jennifer Friedman, Lynne M Bird, Richard Haas, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 90) with videos related to
Sort By:
Page
of 9
Movement Disorders Clinical Practice
|
September 13, 2021
Commentary: Galactosemia Diagnosis by Whole Exome Sequencing Later in Life
Jennifer Friedman, Sara Lucas-Del-Pozo, David Moreno-Martinez, et al.
The American Journal of Pathology
|
October 5, 2010
Sera from preeclampsia patients elicit symptoms of human disease in mice and provide a basis for an in vitro predictive assay
Satyan Kalkunte, Roland Boij, Wendy Norris, et al.
Clinical Genetics
|
October 5, 2024
Consolidating the Role of Mutated ATP2B2 in Neurodevelopmental and Cerebellar Pathologies
Antonia M Stehr, Jerica Lenberg, Jennifer Friedman, et al.
Culture, Health & Sexuality
|
April 26, 2019
Experiences with abortion counselling in Mexico City and Colombia: addressing women's fears and concerns
Brianna Keefe-Oates, Shelly Makleff, Eleuthera Sa, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
November 27, 2014
Assessment of safety in newborns of mothers participating in clinical trials of vaccines administered during pregnancy
Flor M Munoz, Leonard E Weisman, Jennifer S Read, et al.
HGG Advances
|
October 27, 2025
Splicing and frameshift variants in QSER1 may be involved in developmental phenotypes
Megan C Fischer, Linda M Reis, Jerica Lenberg, et al.
Nature Chemical Biology
|
December 21, 2021
Characterization of a patient-derived variant of GPX4 for precision therapy
Hengrui Liu, Farhad Forouhar, Tobias Seibt, et al.
Human Molecular Genetics
|
October 8, 2021
Caenorhabditis elegans provides an efficient drug screening platform for GNAO1-related disorders and highlights the potential role of caffeine in controlling dyskinesia
Martina Di Rocco, Serena Galosi, Enrico Lanza, et al.
Pediatric Neurology
|
October 18, 2024
The Face and Features of RNU4-2: A New, Common, Recognizable, Yet Hidden Neurodevelopmental Disorder
Kristen Barbour, Matthew N Bainbridge, Kristen Wigby, et al.
Molecular Genetics & Genomic Medicine
|
June 2, 2021
Ending a diagnostic odyssey: Moving from exome to genome to identify cockayne syndrome
Jennifer Friedman, Lynne M Bird, Richard Haas, et al.
Page
of 9