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Anna Zachariou

Showing results (11-20 of 29) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 13, 2019
Null variants and deletions in BRWD3 cause an X-linked syndrome of mild-moderate intellectual disability, macrocephaly, and obesity: A series of 17 patientsPhilip J Ostrowski, Anna Zachariou, Chey Loveday, et al.
American Journal of Medical Genetics. Part A|February 23, 2019
EED and EZH2 constitutive variants: A study to expand the Cohen-Gibson syndrome phenotype and contrast it with Weaver syndromeSara Griffiths, Chey Loveday, Anna Zachariou, et al.
Nature Communications|August 8, 2014
Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumourSandra Hanks, Elizabeth R Perdeaux, Sheila Seal, et al.
Nature Genetics|May 30, 2017
Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregationShawn Yost, Bas de Wolf, Sandra Hanks, et al.
Nature Genetics|March 12, 2014
Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disabilityKatrina Tatton-Brown, Sheila Seal, Elise Ruark, et al.
Nature Genetics|November 10, 2015
Mutations in the transcriptional repressor REST predispose to Wilms tumorShazia S Mahamdallie, Sandra Hanks, Kristen L Karlin, et al.
Nature Genetics|March 30, 2016
Corrigendum: Mutations in the transcriptional repressor REST predispose to Wilms tumorShazia S Mahamdallie, Sandra Hanks, Kristen L Karlin, et al.
The Lancet. Child & Adolescent Health|March 20, 2019
Identification of new Wilms tumour predisposition genes: an exome sequencing studyShazia Mahamdallie, Shawn Yost, Emma Poyastro-Pearson, et al.
Oncotarget|January 8, 2019
Correction: Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human heightKatrina Tatton-Brown, Sandra Hanks, Elise Ruark, et al.
Oncotarget|December 23, 2011
Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human heightKatrina Tatton-Brown, Sandra Hanks, Elise Ruark, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 13, 2019
Null variants and deletions in BRWD3 cause an X-linked syndrome of mild-moderate intellectual disability, macrocephaly, and obesity: A series of 17 patientsPhilip J Ostrowski, Anna Zachariou, Chey Loveday, et al.
American Journal of Medical Genetics. Part A|February 23, 2019
EED and EZH2 constitutive variants: A study to expand the Cohen-Gibson syndrome phenotype and contrast it with Weaver syndromeSara Griffiths, Chey Loveday, Anna Zachariou, et al.
Nature Communications|August 8, 2014
Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumourSandra Hanks, Elizabeth R Perdeaux, Sheila Seal, et al.
Nature Genetics|May 30, 2017
Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregationShawn Yost, Bas de Wolf, Sandra Hanks, et al.
Nature Genetics|March 12, 2014
Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disabilityKatrina Tatton-Brown, Sheila Seal, Elise Ruark, et al.
Nature Genetics|November 10, 2015
Mutations in the transcriptional repressor REST predispose to Wilms tumorShazia S Mahamdallie, Sandra Hanks, Kristen L Karlin, et al.
Nature Genetics|March 30, 2016
Corrigendum: Mutations in the transcriptional repressor REST predispose to Wilms tumorShazia S Mahamdallie, Sandra Hanks, Kristen L Karlin, et al.
The Lancet. Child & Adolescent Health|March 20, 2019
Identification of new Wilms tumour predisposition genes: an exome sequencing studyShazia Mahamdallie, Shawn Yost, Emma Poyastro-Pearson, et al.
Oncotarget|January 8, 2019
Correction: Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human heightKatrina Tatton-Brown, Sandra Hanks, Elise Ruark, et al.
Oncotarget|December 23, 2011
Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human heightKatrina Tatton-Brown, Sandra Hanks, Elise Ruark, et al.
Pageof 3