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American Journal of Medical Genetics. Part A
|
December 22, 2017
A novel SAMD9 mutation causing MIRAGE syndrome: An expansion and review of phenotype, dysmorphology, and natural history
Lauren Jeffries, Hirohito Shima, Weizhen Ji, et al.
Molecular Autism
|
May 3, 2018
Abnormal coherence and sleep composition in children with Angelman syndrome: a retrospective EEG study
Hanna den Bakker, Michael S Sidorov, Zheng Fan, et al.
Annals of Clinical and Translational Neurology
|
May 28, 2021
Delta power robustly predicts cognitive function in Angelman syndrome
Lauren M Ostrowski, Elizabeth R Spencer, Lynne M Bird, et al.
Journal of Neurodevelopmental Disorders
|
July 21, 2017
Erratum to: Delta rhythmicity is a reliable EEG biomarker in Angelman syndrome: a parallel mouse and human analysis
Michael S Sidorov, Gina M Deck, Marjan Dolatshahi, et al.
Journal of Neurodevelopmental Disorders
|
May 16, 2017
Delta rhythmicity is a reliable EEG biomarker in Angelman syndrome: a parallel mouse and human analysis
Michael S Sidorov, Gina M Deck, Marjan Dolatshahi, et al.
American Journal of Medical Genetics. Part A
|
June 24, 2020
Genetic diagnoses and associated anomalies in fetuses prenatally diagnosed with esophageal atresia
Mersedeh Rohanizadegan, Sarah Tracy, Carolina I Galarreta, et al.
Orphanet Journal of Rare Diseases
|
October 24, 2019
A placebo-controlled trial of folic acid and betaine in identical twins with Angelman syndrome
Julia Han, Terry Jo Bichell, Stephanie Golden, et al.
American Journal of Medical Genetics. Part A
|
September 25, 2018
Heterozygous WNT1 variant causing a variable bone phenotype
Shatha Alhamdi, Yi-Chien Lee, Shimul Chowdhury, et al.
Molecular Psychiatry
|
August 15, 2020
Angelman syndrome genotypes manifest varying degrees of clinical severity and developmental impairment
Marius Keute, Meghan T Miller, Michelle L Krishnan, et al.
European Journal of Human Genetics : EJHG
|
May 25, 2007
Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations
Trilochan Sahoo, Carlos A Bacino, Jennifer R German, et al.
Page
of 12
Search research articles
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Showing results (41-50 of 120) with videos related to
Sort By:
Page
of 12
American Journal of Medical Genetics. Part A
|
December 22, 2017
A novel SAMD9 mutation causing MIRAGE syndrome: An expansion and review of phenotype, dysmorphology, and natural history
Lauren Jeffries, Hirohito Shima, Weizhen Ji, et al.
Molecular Autism
|
May 3, 2018
Abnormal coherence and sleep composition in children with Angelman syndrome: a retrospective EEG study
Hanna den Bakker, Michael S Sidorov, Zheng Fan, et al.
Annals of Clinical and Translational Neurology
|
May 28, 2021
Delta power robustly predicts cognitive function in Angelman syndrome
Lauren M Ostrowski, Elizabeth R Spencer, Lynne M Bird, et al.
Journal of Neurodevelopmental Disorders
|
July 21, 2017
Erratum to: Delta rhythmicity is a reliable EEG biomarker in Angelman syndrome: a parallel mouse and human analysis
Michael S Sidorov, Gina M Deck, Marjan Dolatshahi, et al.
Journal of Neurodevelopmental Disorders
|
May 16, 2017
Delta rhythmicity is a reliable EEG biomarker in Angelman syndrome: a parallel mouse and human analysis
Michael S Sidorov, Gina M Deck, Marjan Dolatshahi, et al.
American Journal of Medical Genetics. Part A
|
June 24, 2020
Genetic diagnoses and associated anomalies in fetuses prenatally diagnosed with esophageal atresia
Mersedeh Rohanizadegan, Sarah Tracy, Carolina I Galarreta, et al.
Orphanet Journal of Rare Diseases
|
October 24, 2019
A placebo-controlled trial of folic acid and betaine in identical twins with Angelman syndrome
Julia Han, Terry Jo Bichell, Stephanie Golden, et al.
American Journal of Medical Genetics. Part A
|
September 25, 2018
Heterozygous WNT1 variant causing a variable bone phenotype
Shatha Alhamdi, Yi-Chien Lee, Shimul Chowdhury, et al.
Molecular Psychiatry
|
August 15, 2020
Angelman syndrome genotypes manifest varying degrees of clinical severity and developmental impairment
Marius Keute, Meghan T Miller, Michelle L Krishnan, et al.
European Journal of Human Genetics : EJHG
|
May 25, 2007
Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations
Trilochan Sahoo, Carlos A Bacino, Jennifer R German, et al.
Page
of 12