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American Journal of Medical Genetics. Part A
|
April 23, 2018
Williams-Beuren syndrome in diverse populations
Paul Kruszka, Antonio R Porras, Deise Helena de Souza, et al.
American Journal of Medical Genetics. Part A
|
October 24, 2020
Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome
David A Dyment, Anne O'Donnell-Luria, Pankaj B Agrawal, et al.
Science (New York, N.Y.)
|
October 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiC
Florian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan, et al.
Nature Cell Biology
|
July 14, 2015
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes
Gabrielle Wheway, Miriam Schmidts, Dorus A Mans, et al.
American Journal of Human Genetics
|
April 28, 2021
Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism
Maya Chopra, Meriel McEntagart, Jill Clayton-Smith, et al.
American Journal of Human Genetics
|
August 4, 2015
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
Lot Snijders Blok, Erik Madsen, Jane Juusola, et al.
Nature Communications
|
February 17, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Lot Snijders Blok, Justine Rousseau, Joanna Twist, et al.
Nature Communications
|
November 7, 2018
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Lot Snijders Blok, Justine Rousseau, Joanna Twist, et al.
Nature Communications
|
May 4, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Lot Snijders Blok, Justine Rousseau, Joanna Twist, et al.
Human Molecular Genetics
|
January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
Frank J Kaiser, Morad Ansari, Diana Braunholz, et al.
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Search research articles
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Showing results (141-150 of 156) with videos related to
Sort By:
Page
of 16
American Journal of Medical Genetics. Part A
|
April 23, 2018
Williams-Beuren syndrome in diverse populations
Paul Kruszka, Antonio R Porras, Deise Helena de Souza, et al.
American Journal of Medical Genetics. Part A
|
October 24, 2020
Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome
David A Dyment, Anne O'Donnell-Luria, Pankaj B Agrawal, et al.
Science (New York, N.Y.)
|
October 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiC
Florian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan, et al.
Nature Cell Biology
|
July 14, 2015
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes
Gabrielle Wheway, Miriam Schmidts, Dorus A Mans, et al.
American Journal of Human Genetics
|
April 28, 2021
Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism
Maya Chopra, Meriel McEntagart, Jill Clayton-Smith, et al.
American Journal of Human Genetics
|
August 4, 2015
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
Lot Snijders Blok, Erik Madsen, Jane Juusola, et al.
Nature Communications
|
February 17, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Lot Snijders Blok, Justine Rousseau, Joanna Twist, et al.
Nature Communications
|
November 7, 2018
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Lot Snijders Blok, Justine Rousseau, Joanna Twist, et al.
Nature Communications
|
May 4, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Lot Snijders Blok, Justine Rousseau, Joanna Twist, et al.
Human Molecular Genetics
|
January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
Frank J Kaiser, Morad Ansari, Diana Braunholz, et al.
Page
of 16