{"id":556,"date":"2022-01-01T15:19:21","date_gmt":"2022-01-01T15:19:21","guid":{"rendered":"https:\/\/shubhradiagnostics.com\/?page_id=556"},"modified":"2022-01-01T15:44:04","modified_gmt":"2022-01-01T15:44:04","slug":"cytogenetics","status":"publish","type":"page","link":"https:\/\/shubhradiagnostics.com\/?page_id=556","title":{"rendered":"CYTOGENETICS"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"556\" class=\"elementor elementor-556\" data-elementor-settings=\"[]\">\n\t\t\t\t\t\t\t<div class=\"elementor-section-wrap\">\n\t\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-b8321b8 elementor-section-stretched elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"b8321b8\" data-element_type=\"section\" data-settings=\"{&quot;stretch_section&quot;:&quot;section-stretched&quot;}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-4333b5c\" data-id=\"4333b5c\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-3160bc3 elementor-widget elementor-widget-text-editor\" data-id=\"3160bc3\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<style>\/*! elementor - v3.5.0 - 12-12-2021 *\/\n.elementor-widget-text-editor.elementor-drop-cap-view-stacked .elementor-drop-cap{background-color:#818a91;color:#fff}.elementor-widget-text-editor.elementor-drop-cap-view-framed .elementor-drop-cap{color:#818a91;border:3px solid;background-color:transparent}.elementor-widget-text-editor:not(.elementor-drop-cap-view-default) .elementor-drop-cap{margin-top:8px}.elementor-widget-text-editor:not(.elementor-drop-cap-view-default) .elementor-drop-cap-letter{width:1em;height:1em}.elementor-widget-text-editor .elementor-drop-cap{float:left;text-align:center;line-height:1;font-size:50px}.elementor-widget-text-editor .elementor-drop-cap-letter{display:inline-block}<\/style>\t\t\t\t<table><tbody><tr><td width=\"86\"><p><strong>Test Code<\/strong><\/p><\/td><td width=\"188\"><p><strong>Test Name<\/strong><\/p><\/td><td width=\"335\"><p><strong>Test Detail<\/strong><\/p><\/td><td width=\"77\"><p><strong>MRP<\/strong><\/p><\/td><\/tr><tr><td width=\"86\"><p>SCG10009<\/p><\/td><td width=\"188\"><p>Blood Karyotyping Single<\/p><\/td><td width=\"335\"><p>\u00a0<\/p><\/td><td width=\"77\"><p>3300<\/p><\/td><\/tr><tr><td width=\"86\"><p>SCG10005<\/p><\/td><td width=\"188\"><p>Chromosomal Breakage Syndrome<\/p><\/td><td width=\"335\"><p>\u00a0<\/p><\/td><td width=\"77\"><p>7150<\/p><\/td><\/tr><tr><td width=\"86\"><p>SCG10008<\/p><\/td><td width=\"188\"><p>Chromosomal Studies (Fanconi&#8217;s Anemia)<\/p><\/td><td width=\"335\"><p>\u00a0<\/p><\/td><td width=\"77\"><p>7150<\/p><\/td><\/tr><tr><td width=\"86\"><p>SCG10002<\/p><\/td><td width=\"188\"><p>Chromosome Analysis (Genetic Disorders)<\/p><\/td><td width=\"335\"><p>\u00a0<\/p><\/td><td width=\"77\"><p>3300<\/p><\/td><\/tr><tr><td width=\"86\"><p>SCG10001<\/p><\/td><td width=\"188\"><p>Chromosome Analysis (Haematological<\/p><p>Malignancy)<\/p><\/td><td width=\"335\"><p>\u00a0<\/p><\/td><td width=\"77\"><p>3300<\/p><\/td><\/tr><tr><td width=\"86\"><p>SCG10003<\/p><\/td><td width=\"188\"><p>Chromosome Analysis (Married Couple)<\/p><\/td><td width=\"335\"><p>\u00a0<\/p><\/td><td width=\"77\"><p>6050<\/p><\/td><\/tr><tr><td width=\"86\"><p>SCG10004<\/p><\/td><td width=\"188\"><p>Chromosome Analysis (POC)<\/p><\/td><td width=\"335\"><p>\u00a0<\/p><\/td><td width=\"77\"><p>4400<\/p><\/td><\/tr><tr><td colspan=\"4\" width=\"686\"><p><strong>ComboQuest Panels<\/strong><\/p><\/td><\/tr><tr><td width=\"86\"><p><strong>Test Code<\/strong><\/p><\/td><td width=\"188\"><p><strong>Test Name<\/strong><\/p><\/td><td width=\"335\"><p><strong>Test Detail<\/strong><\/p><\/td><td width=\"77\"><p><strong>MRP<\/strong><\/p><\/td><\/tr><tr><td width=\"86\"><p>RP10003<\/p><\/td><td width=\"188\"><p>Acute Leukemia Comprehensive &amp; Karyotype<\/p><\/td><td width=\"335\"><p>Acute Leukemia Comprehensive Diagnosis, Chromosome Analysis<\/p><p>(Haem.Malignancy)<\/p><\/td><td width=\"77\"><p>13090<\/p><\/td><\/tr><tr><td width=\"86\"><p>RP10008<\/p><\/td><td width=\"188\"><p>ALL Characterization &amp; Karyotype Combo<\/p><\/td><td width=\"335\"><p>ALL Characterization Panel, Chromosome Analysis (Haem.Malignancy)<\/p><\/td><td width=\"77\"><p>11440<\/p><\/td><\/tr><tr><td width=\"86\"><p>RP10006<\/p><\/td><td width=\"188\"><p>AML Characterization &amp; Karyotyping Combo<\/p><\/td><td width=\"335\"><p>AML Characterization Panel, Chromosome Analysis (Haem.Malignancy)<\/p><\/td><td width=\"77\"><p>10890<\/p><\/td><\/tr><tr><td width=\"86\"><p>RP10039<\/p><\/td><td width=\"188\"><p>CLL Comprehensive &amp; Karyotype Combo<\/p><\/td><td width=\"335\"><p>CLL Characterization Panel, Chromosome Analysis (Haem.Malignancy)<\/p><\/td><td width=\"77\"><p>14080<\/p><\/td><\/tr><tr><td width=\"86\"><p>RP10040<\/p><\/td><td width=\"188\"><p>Lymphoma Comprehensive &amp; Karyotype<\/p><p>Combo<\/p><\/td><td width=\"335\"><p>Lymphoma Diagnostic Panel, Chromosome Analysis (Haem.Malignancy)<\/p><\/td><td width=\"77\"><p>13090<\/p><\/td><\/tr><tr><td width=\"86\"><p>RP10007<\/p><\/td><td width=\"188\"><p>T, B Myeloid &amp; Karyotype Combo Panel<\/p><\/td><td width=\"335\"><p>Acute Leukemia -T, B or Myeloid, Chromosome Analysis (Haem.Malignancy)<\/p><\/td><td width=\"77\"><p>9240<\/p><\/td><\/tr><tr><td width=\"86\"><p>SCG10010<\/p><\/td><td width=\"188\"><p>t11;22 (Ewings Sarcoma)<\/p><\/td><td width=\"335\"><p>\u00a0<\/p><\/td><td width=\"77\"><p>7150<\/p><\/td><\/tr><\/tbody><\/table>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>Test Code Test Name Test Detail MRP SCG10009 Blood Karyotyping Single \u00a0 3300 SCG10005 Chromosomal Breakage Syndrome \u00a0 7150 SCG10008 Chromosomal Studies (Fanconi&#8217;s Anemia) \u00a0 7150 SCG10002 Chromosome Analysis (Genetic Disorders) \u00a0 3300 SCG10001 Chromosome Analysis (Haematological Malignancy) \u00a0 3300 SCG10003 Chromosome Analysis (Married Couple) \u00a0 6050 SCG10004 Chromosome Analysis (POC) \u00a0 4400 ComboQuest Panels [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"om_disable_all_campaigns":false},"_links":{"self":[{"href":"https:\/\/shubhradiagnostics.com\/index.php?rest_route=\/wp\/v2\/pages\/556"}],"collection":[{"href":"https:\/\/shubhradiagnostics.com\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/shubhradiagnostics.com\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/shubhradiagnostics.com\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/shubhradiagnostics.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=556"}],"version-history":[{"count":4,"href":"https:\/\/shubhradiagnostics.com\/index.php?rest_route=\/wp\/v2\/pages\/556\/revisions"}],"predecessor-version":[{"id":596,"href":"https:\/\/shubhradiagnostics.com\/index.php?rest_route=\/wp\/v2\/pages\/556\/revisions\/596"}],"wp:attachment":[{"href":"https:\/\/shubhradiagnostics.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=556"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}