hgmd cf.ac.uk

HGMD home page

The Human Gene Mutation Database. At the Institute of Medical Genetics in Cardiff. The Human Gene Mutation Database HGMD. Represents an attempt to collate all known published gene lesions responsible for human inherited disease and is maintained in Cardiff by D.N. Cooper, E.V. Ball, P.D. Stenson, A.D. Phillips, K. Evans, S. Heywood, M.J. Hayden, L. Azevedo, M.E. Mort and M. Hussain. Please note that this less up-to-date public version of our database is freely available only to registered. Standard H.
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This site hgmd.cf.ac.uk presently has an average traffic classification of zero (the smaller the superior). We have probed three pages within the website hgmd.cf.ac.uk and found seventy-four websites interfacing with hgmd.cf.ac.uk.
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74

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LINKS TO WEB PAGE

TIGEM Bioinformatics Core

XIX Convention TELETHON Riva del Garda 13-15 March 2017. Welcome to the TIGEM Bioinformatics Services. Our team of bioinformaticians, statisticians and biologists will work with you step by step from data analysis to manuscript preparation. Results are delivered in a secure and comprehensive manner and are the ideal starting point for your downstream interpretation.

Biomedicina Hoy

Biomedicine - Биомедицина - Biomedizin - Biomédecine - الطب الحيوي. Jueves, 28 de septiembre de 2017. A la izquierda hacer clic donde dice. Leer la Historia de los modelos atómicos. Luego, en la parte superior hacer clic en la viñeta Estructura. Leer y responder preguntas, para luego anotar la calificación obtenida. Después, en la parte superior hacer clic en Construir átomos.

Laboratorio Elea - Industria Farmacéutica Argentina

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European Society for Pigment Cell Research ESPCR

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FinDis - Home

Is a centralized resource for cross-referenced information on disease mutations enriched in the Finnish population. FinDis provides up-to-date information on the 36 monogenic diseases belonging to the Finnish disease heritage. Prevalence or incidence and a short description of clinical symptoms. Genetic locus and a molecular description for identified mutations. Disease allele frequencies typically reported for Finnish mutations. Read About the FinDis project.

Instituto de genética UNAL

Grupo Biodiversidad y Conservación Genética. Grupo Bioinformática y Biología de Sistemas Computacional. Grupo Biofísica de la Señalización Celular. Grupo Control Genético en Salud Animal. Grupo Crecimiento y Desarrollo Craneofacial. Grupo Genética de Poblaciones e Identificación. Grupo Identificación Humana e Inmunogenética. Grupo Ingeniería Genética de Plantas. Grupo Inmunología Evolutiva e Inmunogenética.

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HGMD.CF.AC.UK HOST

We diagnosed that a lone root page on hgmd.cf.ac.uk took six hundred and five milliseconds to download. We could not observe a SSL certificate, so therefore we consider this site not secure.
Load time
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Internet Address
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I discovered that this domain is employing the Apache os.

PAGE TITLE

HGMD home page

DESCRIPTION

The Human Gene Mutation Database. At the Institute of Medical Genetics in Cardiff. The Human Gene Mutation Database HGMD. Represents an attempt to collate all known published gene lesions responsible for human inherited disease and is maintained in Cardiff by D.N. Cooper, E.V. Ball, P.D. Stenson, A.D. Phillips, K. Evans, S. Heywood, M.J. Hayden, L. Azevedo, M.E. Mort and M. Hussain. Please note that this less up-to-date public version of our database is freely available only to registered. Standard H.

CONTENT

This site states the following, "At the Institute of Medical Genetics in Cardiff." Our analyzers observed that the web page also stated " The Human Gene Mutation Database HGMD." The Website also stated " Represents an attempt to collate all known published gene lesions responsible for human inherited disease and is maintained in Cardiff by D. Please note that this less up-to-date public version of our database is freely available only to registered." The website's header had human gene mutation database inherited disease causing associated functional polymorphism HGMD as the most important keyword.

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