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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 18, 2020
GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder
Christine Shieh, Natasha Jones, Brigitte Vanle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 13, 2020
Correction: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder
Christine Shieh, Natasha Jones, Brigitte Vanle, et al.
Human Mutation
|
February 7, 2015
De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypes
María Concepción Gil-Rodríguez, Matthew A Deardorff, Morad Ansari, et al.
Journal of Medical Genetics
|
August 16, 2014
Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism
Morad Ansari, Gemma Poke, Quentin Ferry, et al.
Nature Genetics
|
August 2, 2016
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
Alejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, et al.
Nature Genetics
|
May 27, 2017
Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome
Natalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Nature Genetics
|
January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome
Natalie D Shaw, Harrison Brand, Zachary A Kupchinsky, 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.
American Journal of Human Genetics
|
September 6, 2020
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations
Dervla M Connaughton, Rufeng Dai, Danielle J Owen, et al.
American Journal of Human Genetics
|
November 4, 2017
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
Fadi F Hamdan, Candace T Myers, Patrick Cossette, et al.
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Search research articles
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Showing results (141-150 of 153) with videos related to
Sort By:
Page
of 16
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 18, 2020
GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder
Christine Shieh, Natasha Jones, Brigitte Vanle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 13, 2020
Correction: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder
Christine Shieh, Natasha Jones, Brigitte Vanle, et al.
Human Mutation
|
February 7, 2015
De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypes
María Concepción Gil-Rodríguez, Matthew A Deardorff, Morad Ansari, et al.
Journal of Medical Genetics
|
August 16, 2014
Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism
Morad Ansari, Gemma Poke, Quentin Ferry, et al.
Nature Genetics
|
August 2, 2016
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
Alejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, et al.
Nature Genetics
|
May 27, 2017
Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome
Natalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Nature Genetics
|
January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome
Natalie D Shaw, Harrison Brand, Zachary A Kupchinsky, 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.
American Journal of Human Genetics
|
September 6, 2020
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations
Dervla M Connaughton, Rufeng Dai, Danielle J Owen, et al.
American Journal of Human Genetics
|
November 4, 2017
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
Fadi F Hamdan, Candace T Myers, Patrick Cossette, et al.
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of 16