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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 patients
Philip 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 syndrome
Sara Griffiths, Chey Loveday, Anna Zachariou, et al.
Nature Communications
|
August 8, 2014
Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour
Sandra Hanks, Elizabeth R Perdeaux, Sheila Seal, et al.
Nature Genetics
|
May 30, 2017
Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation
Shawn 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 disability
Katrina Tatton-Brown, Sheila Seal, Elise Ruark, et al.
Nature Genetics
|
November 10, 2015
Mutations in the transcriptional repressor REST predispose to Wilms tumor
Shazia S Mahamdallie, Sandra Hanks, Kristen L Karlin, et al.
Nature Genetics
|
March 30, 2016
Corrigendum: Mutations in the transcriptional repressor REST predispose to Wilms tumor
Shazia 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 study
Shazia 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 height
Katrina Tatton-Brown, Sandra Hanks, Elise Ruark, et al.
Oncotarget
|
December 23, 2011
Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height
Katrina Tatton-Brown, Sandra Hanks, Elise Ruark, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 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 patients
Philip 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 syndrome
Sara Griffiths, Chey Loveday, Anna Zachariou, et al.
Nature Communications
|
August 8, 2014
Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour
Sandra Hanks, Elizabeth R Perdeaux, Sheila Seal, et al.
Nature Genetics
|
May 30, 2017
Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation
Shawn 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 disability
Katrina Tatton-Brown, Sheila Seal, Elise Ruark, et al.
Nature Genetics
|
November 10, 2015
Mutations in the transcriptional repressor REST predispose to Wilms tumor
Shazia S Mahamdallie, Sandra Hanks, Kristen L Karlin, et al.
Nature Genetics
|
March 30, 2016
Corrigendum: Mutations in the transcriptional repressor REST predispose to Wilms tumor
Shazia 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 study
Shazia 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 height
Katrina Tatton-Brown, Sandra Hanks, Elise Ruark, et al.
Oncotarget
|
December 23, 2011
Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height
Katrina Tatton-Brown, Sandra Hanks, Elise Ruark, et al.
Page
of 3