umr910.timone univ-mrs.fr

UMRS910

Medical Genetics and Functional Genomics. Mutations in the FAT1 gene associated with FSHD. Molecular diagnosis by NGS of Distal Myopathies. 3 two years postdoctoral positions are currently available in our institute. 3 two years post-doctoral positions are available immediately to set-up a Mediterranean Research Network for the study of rare diseases in the Mediterranean area and identify new genes in rare autosomal recessive diseases by Next Generation Sequencing of patients from consanguineous families.

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The web page umr910.timone.univ-mrs.fr presently has a traffic ranking of zero (the smaller the higher page views). We have crawled nine pages inside the web page umr910.timone.univ-mrs.fr and found eleven websites referring to umr910.timone.univ-mrs.fr. We were able to precure one social communication platforms possessed by this website.
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UMR910.TIMONE.UNIV-MRS.FR TRAFFIC

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LINKS TO UMR910.TIMONE.UNIV-MRS.FR

2013 International Nevus Expert Meeting

2013 Expert Meeting on CMN and NCM. Welcome to the second edition of the International Expert Meeting on Large Congenital Melanocytic Nevi. To report results and observations. On CMN, NCM and pediatric melanoma. To stimulate discussion and foster collaboration. To report to the medical and scientific community. Are you a reconstructive plastic surgeon.

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WHAT DOES UMR910.TIMONE.UNIV-MRS.FR LOOK LIKE?

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UMR910.TIMONE.UNIV-MRS.FR SERVER

I caught that the main page on umr910.timone.univ-mrs.fr took one thousand two hundred and ninety-seven milliseconds to download. I could not find a SSL certificate, so therefore our parsers consider umr910.timone.univ-mrs.fr not secure.
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SERVER SOFTWARE AND ENCODING

We caught that umr910.timone.univ-mrs.fr is weilding the Apache/2.2.9 (Debian) PHP/5.2.6-1+lenny16 with Suhosin-Patch server.

SITE TITLE

UMRS910

DESCRIPTION

Medical Genetics and Functional Genomics. Mutations in the FAT1 gene associated with FSHD. Molecular diagnosis by NGS of Distal Myopathies. 3 two years postdoctoral positions are currently available in our institute. 3 two years post-doctoral positions are available immediately to set-up a Mediterranean Research Network for the study of rare diseases in the Mediterranean area and identify new genes in rare autosomal recessive diseases by Next Generation Sequencing of patients from consanguineous families.

PARSED CONTENT

The web page states the following, "Mutations in the FAT1 gene associated with FSHD." I viewed that the web page said " Molecular diagnosis by NGS of Distal Myopathies." They also said " 3 two years postdoctoral positions are currently available in our institute. 3 two years post-doctoral positions are available immediately to set-up a Mediterranean Research Network for the study of rare diseases in the Mediterranean area and identify new genes in rare autosomal recessive diseases by Next Generation Sequencing of patients from consanguineous families." The meta header had disease as the first search term. This keyword is followed by rare disease, research unit, and database which isn't as important as disease. The other words they uses is mutations. animal model is included and could not be viewed by search crawlers.

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