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Journal of Medical Genetics
|
May 15, 2017
Genetic causes of optic nerve hypoplasia
Chun-An Chen, Jiani Yin, Richard Alan Lewis, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 5, 2024
From newborn screening to genomic medicine: challenges and suggestions on how to incorporate genomic newborn screening in public health programs
Nicola Dikow, Beate Ditzen, Stefan Kölker, et al.
Progress in Neurobiology
|
July 23, 2022
Emerging role of astrocytes in oxytocin-mediated control of neural circuits and brain functions
Angel Baudon, Etienne Clauss Creusot, Ferdinand Althammer, et al.
American Journal of Medical Genetics. Part A
|
September 25, 2021
Parental perceptions of genetic testing for children with autism spectrum disorders
Heather M Lucas, Andrea M Lewis, Philip J Lupo, et al.
Hereditary Cancer in Clinical Practice
|
July 3, 2023
BRCA1/2 potential founder variants in the Jordanian population: an opportunity for a customized screening panel
Olfat Ahmad, Christian Sutter, Steffen Hirsch, et al.
American Journal of Medical Genetics. Part A
|
July 12, 2025
Unraveling the Genomic Architecture of Supernumerary (Iso-)Dicentric Chromosomes in Dup15q Syndrome: Insight From a Systematic Literature-Based Study
Sebastian Burkart, Markus Ries, Verena Romero, et al.
Journal of Autism and Developmental Disorders
|
January 13, 2016
Assessment of Cognitive Outcome Measures in Teenagers with 15q13.3 Microdeletion Syndrome
Emeline Crutcher, May Ali, John Harrison, et al.
Photodermatology, Photoimmunology & Photomedicine
|
November 8, 2007
Hans Gunther and his disease
Pankaj Madan, Christian P Schaaf, Prem Vardhan, et al.
American Journal of Medical Genetics. Part A
|
April 15, 2025
A Case of Prader-Willi Syndrome With a Deletion Including MAGEL2, NDN, and MKRN3, but Excluding SNRPN and SNORD116
Jannis Buecking, Yu An, Weimin Bi, et al.
American Journal of Medical Genetics. Part A
|
June 18, 2025
Phenotypical and Genotypical Expansion of Autosomal-Dominant KDM1A-Related Neurodevelopmental Disorder Spectrum: A Case Report
Sebastian Burkart, Melanie Spanjaard, Lilian Kaufmann, et al.
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of 18
Search research articles
Search
Showing results (31-40 of 179) with videos related to
Sort By:
Page
of 18
Journal of Medical Genetics
|
May 15, 2017
Genetic causes of optic nerve hypoplasia
Chun-An Chen, Jiani Yin, Richard Alan Lewis, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 5, 2024
From newborn screening to genomic medicine: challenges and suggestions on how to incorporate genomic newborn screening in public health programs
Nicola Dikow, Beate Ditzen, Stefan Kölker, et al.
Progress in Neurobiology
|
July 23, 2022
Emerging role of astrocytes in oxytocin-mediated control of neural circuits and brain functions
Angel Baudon, Etienne Clauss Creusot, Ferdinand Althammer, et al.
American Journal of Medical Genetics. Part A
|
September 25, 2021
Parental perceptions of genetic testing for children with autism spectrum disorders
Heather M Lucas, Andrea M Lewis, Philip J Lupo, et al.
Hereditary Cancer in Clinical Practice
|
July 3, 2023
BRCA1/2 potential founder variants in the Jordanian population: an opportunity for a customized screening panel
Olfat Ahmad, Christian Sutter, Steffen Hirsch, et al.
American Journal of Medical Genetics. Part A
|
July 12, 2025
Unraveling the Genomic Architecture of Supernumerary (Iso-)Dicentric Chromosomes in Dup15q Syndrome: Insight From a Systematic Literature-Based Study
Sebastian Burkart, Markus Ries, Verena Romero, et al.
Journal of Autism and Developmental Disorders
|
January 13, 2016
Assessment of Cognitive Outcome Measures in Teenagers with 15q13.3 Microdeletion Syndrome
Emeline Crutcher, May Ali, John Harrison, et al.
Photodermatology, Photoimmunology & Photomedicine
|
November 8, 2007
Hans Gunther and his disease
Pankaj Madan, Christian P Schaaf, Prem Vardhan, et al.
American Journal of Medical Genetics. Part A
|
April 15, 2025
A Case of Prader-Willi Syndrome With a Deletion Including MAGEL2, NDN, and MKRN3, but Excluding SNRPN and SNORD116
Jannis Buecking, Yu An, Weimin Bi, et al.
American Journal of Medical Genetics. Part A
|
June 18, 2025
Phenotypical and Genotypical Expansion of Autosomal-Dominant KDM1A-Related Neurodevelopmental Disorder Spectrum: A Case Report
Sebastian Burkart, Melanie Spanjaard, Lilian Kaufmann, et al.
Page
of 18