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Showing results (221-230 of 226) with videos related to

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Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 7, 2018
MSR1 repeats modulate gene expression and affect risk of breast and prostate cancerA M Rose, A Krishan, C F Chakarova, et al.
Nature Genetics|June 1, 1996
Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2D W Johnson, J N Berg, M A Baldwin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 29, 2016
Genome-wide association study of sporadic brain arteriovenous malformationsShantel Weinsheimer, Nasrine Bendjilali, Jeffrey Nelson, et al.
Human Mutation|April 29, 1998
Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null allelesC J Gallione, D J Klaus, E Y Yeh, et al.
Orphanet Journal of Rare Diseases|February 15, 2014
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlationsVeerle Rc Eggens, Peter G Barth, Jikke-Mien F Niermeijer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 30, 2019
De novo and biallelic DEAF1 variants cause a phenotypic spectrumMaria J Nabais Sá, Philip J Jensik, Stacey R McGee, et al.
Pageof 23

Showing results (221-230 of 226) with videos related to

Sort By:
Pageof 23
You have reached the last page of results.This site can display upto 226 results.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 7, 2018
MSR1 repeats modulate gene expression and affect risk of breast and prostate cancerA M Rose, A Krishan, C F Chakarova, et al.
Nature Genetics|June 1, 1996
Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2D W Johnson, J N Berg, M A Baldwin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 29, 2016
Genome-wide association study of sporadic brain arteriovenous malformationsShantel Weinsheimer, Nasrine Bendjilali, Jeffrey Nelson, et al.
Human Mutation|April 29, 1998
Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null allelesC J Gallione, D J Klaus, E Y Yeh, et al.
Orphanet Journal of Rare Diseases|February 15, 2014
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlationsVeerle Rc Eggens, Peter G Barth, Jikke-Mien F Niermeijer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 30, 2019
De novo and biallelic DEAF1 variants cause a phenotypic spectrumMaria J Nabais Sá, Philip J Jensik, Stacey R McGee, et al.
Pageof 23