[vc_row anchor=”genetic”][vc_column][vc_row_inner][vc_column_inner width=”1\/3″][vc_single_image image=”25″ img_size=”full” alignment=”center” style=”vc_box_shadow_circle_2″][\/vc_column_inner][vc_column_inner width=”2\/3″]

Genetic studies<\/h2><\/div>
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content_placement=”middle” gap=”30″][vc_column_inner width=”2\/3″][vc_column_text]by Sanger<\/strong><\/p>\n
\n
Hereditary Hyperferritinemia with cataracts Syndrome (HHCS, exon 1 FTL) (Code 20050)<\/a><\/li>\n
Initial study for Hereditary Hemochromatosis (C282Y mutation in HFE gene) (Code 20051)<\/a><\/li>\n
Familial Genetic study of a known mutation by Sanger, study of one\/two\/three mutation\/s in one gene (Code 20010, 20020, 20030)<\/a><\/li>\n
Full HBB’s gene Sanger study (Code 20052)<\/a><\/li>\n<\/ul>\n
[\/vc_column_text][vc_column_text]Data analysis studies<\/strong><\/p>\n
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NGS panel data analysis study (Code 30010)\u00a0<\/a><\/li>\n
Whole Exome Sequencing (WES) data analysis study (Code 30020)<\/a><\/li>\n<\/ul>\n
[\/vc_column_text][\/vc_column_inner][vc_column_inner el_class=”primero” width=”1\/3″]REQUEST<\/span><\/a>[\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row type=”vc_default” bg_type=”bg_color” bg_override=”full” css=”.vc_custom_1497012285234{margin-top: 70px !important;margin-bottom: -70px !important;padding-top: 40px !important;padding-bottom: 70px !important;}” bg_color_value=”#f7f7f7″ el_id=”biochemical”][vc_column][vc_row_inner][vc_column_inner width=”1\/3″][vc_single_image image=”27″ img_size=”full” alignment=”center” style=”vc_box_shadow_circle_2″][\/vc_column_inner][vc_column_inner width=”2\/3″]
Biochemical studies<\/h2><\/div>
<\/span><\/div><\/div>[vc_empty_space][vc_column_text]Biochemical study of serum or plasma hepcidin measurement by ELISA kit (Code 90010)<\/a><\/p>\n
Biochemical study of Labile Plasma Iron (LPI) measurement in serum or plasma (Code 90020)<\/a>[\/vc_column_text]REQUEST<\/span><\/a>[\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row]<\/p>\n","protected":false},"excerpt":{"rendered":"
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