The top documents tagged [disease phenotypes]

MICI: classification et nosologie le point de vue du clinicien Edouard Louis Service de Gastroentérologie, CHU Liège GIGAresearch, Université de Liège
Documents MICI: classification et nosologie le point de vue du clinicien Edouard Louis Service de Gastroentérologie, CHU Liège GIGAresearch, Université de Liège

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X LINKED INHERITANCE. X Linked (XL) disorders are encoded on the X chromosome. Males inherit their X chromosome from their mother, and Y chromosome from
Documents X LINKED INHERITANCE. X Linked (XL) disorders are encoded on the X chromosome. Males inherit their X chromosome from their mother, and Y chromosome from

234 views

Medical bioinformatics: Current trends, industry needs, and core competencies
Science Medical bioinformatics: Current trends, industry needs, and core competencies

353 views

Human developmental-kb-2012
Health & Medicine Human developmental-kb-2012

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Vasculitis nrrheum.2014.89
Documents Vasculitis nrrheum.2014.89

108 views

Variant Calling II
Science Variant Calling II

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Translational bioinformatics at VHIR: Understanding molecular damage in Fabry disease
Documents Translational bioinformatics at VHIR: Understanding molecular damage in Fabry disease

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[Dean_M.]_The_Human_ATP-Binding_Cassette_(ABC)_Tra(BookZZ.org).pdf
Documents [Dean_M.]_The_Human_ATP-Binding_Cassette_(ABC)_Tra(BookZZ.org).pdf

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“10,001 Dalmatians” research programme: Discovery of genetic variants that control human quantitative traits and predispose to diseases Igor Rudan, Mladen
Documents “10,001 Dalmatians” research programme: Discovery of genetic variants that control human quantitative traits and predispose to diseases Igor Rudan, Mladen

224 views

Systems Biology approaches to understanding glutathione metabolism 29 September 2010 Dr Najl Valeyev Edinburgh University of Kent Centre for Molecular
Documents Systems Biology approaches to understanding glutathione metabolism 29 September 2010 Dr Najl Valeyev Edinburgh University of Kent Centre for Molecular

218 views

Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network Ivan Iossifov, Tian Zheng, Miron Baron, T. Conrad
Documents Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network Ivan Iossifov, Tian Zheng, Miron Baron, T. Conrad

215 views

ENCODE 2012. The Human Genome project sequenced “the human genome” “the human genome” that we have labeled as such doesn’t actually exist What we call
Documents ENCODE 2012. The Human Genome project sequenced “the human genome” “the human genome” that we have labeled as such doesn’t actually exist What we call

223 views