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American Journal of Medical Genetics. Part A
|
November 9, 2022
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome
Emma K Baker, Marta Arpone, Minh Bui, et al.
Human Molecular Genetics
|
May 22, 2025
Improving genetic diagnostic yield in familial and sporadic cerebral cavernous malformations: detection of copy number and deep Intronic variants
Neblina Sikta, Samuel Gooley, Timothy E Green, et al.
Scientific Reports
|
February 28, 2018
Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X
Marta Arpone, Emma K Baker, Lesley Bretherton, et al.
Emerging Microbes & Infections
|
June 2, 2018
Antigenic characterization of highly pathogenic avian influenza A(H5N1) viruses with chicken and ferret antisera reveals clade-dependent variation in hemagglutination inhibition profiles
Diep Thi Nguyen, Samuel S Shepard, David Francis Burke, et al.
International Journal of Molecular Sciences
|
August 26, 2023
Molecular Changes in the Brain of the Wintering <i>Calidris pusilla</i> in the Mangroves of the Amazon River Estuary
Patrick Douglas Corrêa Pereira, Ediely Pereira Henrique, Emanuel Ramos da Costa, et al.
Australian and New Zealand Journal of Public Health
|
February 13, 2024
Balancing the risks and benefits of sun exposure: A revised position statement for Australian adults
Rachel E Neale, Victoria Beedle, Peter R Ebeling, et al.
Frontiers in Neuroanatomy
|
November 5, 2019
Differential Change in Hippocampal Radial Astrocytes and Neurogenesis in Shorebirds With Contrasting Migratory Routes
Camila Mendes de Lima, Patrick Douglas Corrêa Pereira, Ediely Pereira Henrique, et al.
JAMA Network Open
|
January 4, 2022
Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic Workflow
David E Godler, Ling Ling, Dinusha Gamage, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 13, 2012
Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study
Yoshimi Inaba, Amy S Herlihy, Charles E Schwartz, et al.
Journal of Neurodevelopmental Disorders
|
December 28, 2019
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
Emma K Baker, Marta Arpone, Solange Aliaga Vera, et al.
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of 18
Search research articles
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Showing results (151-160 of 176) with videos related to
Sort By:
Page
of 18
American Journal of Medical Genetics. Part A
|
November 9, 2022
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome
Emma K Baker, Marta Arpone, Minh Bui, et al.
Human Molecular Genetics
|
May 22, 2025
Improving genetic diagnostic yield in familial and sporadic cerebral cavernous malformations: detection of copy number and deep Intronic variants
Neblina Sikta, Samuel Gooley, Timothy E Green, et al.
Scientific Reports
|
February 28, 2018
Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X
Marta Arpone, Emma K Baker, Lesley Bretherton, et al.
Emerging Microbes & Infections
|
June 2, 2018
Antigenic characterization of highly pathogenic avian influenza A(H5N1) viruses with chicken and ferret antisera reveals clade-dependent variation in hemagglutination inhibition profiles
Diep Thi Nguyen, Samuel S Shepard, David Francis Burke, et al.
International Journal of Molecular Sciences
|
August 26, 2023
Molecular Changes in the Brain of the Wintering <i>Calidris pusilla</i> in the Mangroves of the Amazon River Estuary
Patrick Douglas Corrêa Pereira, Ediely Pereira Henrique, Emanuel Ramos da Costa, et al.
Australian and New Zealand Journal of Public Health
|
February 13, 2024
Balancing the risks and benefits of sun exposure: A revised position statement for Australian adults
Rachel E Neale, Victoria Beedle, Peter R Ebeling, et al.
Frontiers in Neuroanatomy
|
November 5, 2019
Differential Change in Hippocampal Radial Astrocytes and Neurogenesis in Shorebirds With Contrasting Migratory Routes
Camila Mendes de Lima, Patrick Douglas Corrêa Pereira, Ediely Pereira Henrique, et al.
JAMA Network Open
|
January 4, 2022
Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic Workflow
David E Godler, Ling Ling, Dinusha Gamage, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 13, 2012
Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study
Yoshimi Inaba, Amy S Herlihy, Charles E Schwartz, et al.
Journal of Neurodevelopmental Disorders
|
December 28, 2019
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
Emma K Baker, Marta Arpone, Solange Aliaga Vera, et al.
Page
of 18