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International Journal of Molecular Sciences
|
October 22, 2020
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome
Claudine M Kraan, Emma K Baker, Marta Arpone, et al.
American Journal of Medical Genetics. Part A
|
September 21, 2021
Paternal retraction of a fragile X allele to normal size, showing normal function over two generations
Essra Bartlett, Alison D Archibald, David Francis, et al.
Clinical Chemistry
|
April 30, 2014
Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spots
Yoshimi Inaba, Charles E Schwartz, Quang M Bui, et al.
Expert Reviews in Molecular Medicine
|
July 2, 2015
Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis
David E Godler, Yoshimi Inaba, Charles E Schwartz, et al.
Plos One
|
September 1, 2010
A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33
Ryan N Traylor, Damien L Bruno, Trent Burgess, et al.
Diabetes & Metabolism Journal
|
April 30, 2022
Influence of Maternal Diabetes on the Risk of Neurodevelopmental Disorders in Offspring in the Prenatal and Postnatal Periods
Verónica Perea, Xavier Urquizu, Maite Valverde, et al.
European Journal of Human Genetics : EJHG
|
October 10, 2013
Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome
Gabrielle R Wilson, Jasmine Sunley, Katherine R Smith, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation
|
May 2, 2022
Patient Experience in Pancreas-Kidney Transplantation-A Methodological Approach Towards Innovation in an Established Program
Pedro Ventura-Aguiar, Beatriu Bayés-Genís, Antonio J Amor, et al.
European Journal of Human Genetics : EJHG
|
November 10, 2020
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort study
Lilian Downie, Jane Halliday, Rachel Burt, et al.
European Journal of Human Genetics : EJHG
|
December 13, 2019
Exome sequencing in infants with congenital hearing impairment: a population-based cohort study
Lilian Downie, Jane Halliday, Rachel Burt, et al.
Page
of 43
Search research articles
Search
Showing results (301-310 of 430) with videos related to
Sort By:
Page
of 43
International Journal of Molecular Sciences
|
October 22, 2020
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome
Claudine M Kraan, Emma K Baker, Marta Arpone, et al.
American Journal of Medical Genetics. Part A
|
September 21, 2021
Paternal retraction of a fragile X allele to normal size, showing normal function over two generations
Essra Bartlett, Alison D Archibald, David Francis, et al.
Clinical Chemistry
|
April 30, 2014
Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spots
Yoshimi Inaba, Charles E Schwartz, Quang M Bui, et al.
Expert Reviews in Molecular Medicine
|
July 2, 2015
Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis
David E Godler, Yoshimi Inaba, Charles E Schwartz, et al.
Plos One
|
September 1, 2010
A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33
Ryan N Traylor, Damien L Bruno, Trent Burgess, et al.
Diabetes & Metabolism Journal
|
April 30, 2022
Influence of Maternal Diabetes on the Risk of Neurodevelopmental Disorders in Offspring in the Prenatal and Postnatal Periods
Verónica Perea, Xavier Urquizu, Maite Valverde, et al.
European Journal of Human Genetics : EJHG
|
October 10, 2013
Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome
Gabrielle R Wilson, Jasmine Sunley, Katherine R Smith, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation
|
May 2, 2022
Patient Experience in Pancreas-Kidney Transplantation-A Methodological Approach Towards Innovation in an Established Program
Pedro Ventura-Aguiar, Beatriu Bayés-Genís, Antonio J Amor, et al.
European Journal of Human Genetics : EJHG
|
November 10, 2020
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort study
Lilian Downie, Jane Halliday, Rachel Burt, et al.
European Journal of Human Genetics : EJHG
|
December 13, 2019
Exome sequencing in infants with congenital hearing impairment: a population-based cohort study
Lilian Downie, Jane Halliday, Rachel Burt, et al.
Page
of 43