{"id":12705,"date":"2026-02-03T14:20:08","date_gmt":"2026-02-03T11:20:08","guid":{"rendered":"https:\/\/nesiller.com\/carrier-screening\/"},"modified":"2026-10-20T20:27:11","modified_gmt":"2026-10-20T17:27:11","slug":"carrier-screening","status":"publish","type":"page","link":"https:\/\/nesiller.com\/en\/carrier-screening\/","title":{"rendered":"Carrier Screening"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"12705\" class=\"elementor elementor-12705 elementor-9706\" data-elementor-post-type=\"page\">\n\t\t\t\t<div data-ekitparallax=\"{&quot;ekit_section_parallax_bg&quot;:&quot;yes&quot;,&quot;ekit_section_parallax_bg_speed&quot;:0.5,&quot;elementor_lazy_load&quot;:&quot;1&quot;}\" class=\"elementor-element elementor-element-fd5084e e-flex e-con-boxed e-con e-parent\" data-id=\"fd5084e\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t<div class=\"elementor-element elementor-element-7c98690 e-con-full e-flex e-con e-child\" data-id=\"7c98690\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-a51483c section-title at-heading-animation at-animation-heading-none elementor-invisible elementor-widget elementor-widget-heading\" data-id=\"a51483c\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;_animation&quot;:&quot;fadeInUp&quot;,&quot;ekit_we_effect_on&quot;:&quot;none&quot;}\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<div class=\"elementor-heading-title elementor-size-default\">Carrier Screening and Reproductive Genetics<\/div>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-b855eae elementor-widget elementor-widget-heading\" data-id=\"b855eae\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;ekit_we_effect_on&quot;:&quot;none&quot;}\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h1 class=\"elementor-heading-title elementor-size-default\">IntelliGene Carrier Screening \/ Reproductive Genetics<\/h1>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-024c3dd elementor-invisible elementor-widget elementor-widget-text-editor\" data-id=\"024c3dd\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;_animation&quot;:&quot;fadeInUp&quot;,&quot;_animation_delay&quot;:200,&quot;ekit_we_effect_on&quot;:&quot;none&quot;}\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>The First Step in Family Planning<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-5ac74e4 e-flex e-con-boxed e-con e-parent\" data-id=\"5ac74e4\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-ce6fc12 elementor-widget elementor-widget-text-editor\" data-id=\"ce6fc12\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;ekit_we_effect_on&quot;:&quot;none&quot;}\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><img decoding=\"async\" class=\"size-medium wp-image-11383 aligncenter\" src=\"https:\/\/nesiller.com\/wp-content\/uploads\/2026\/02\/intelliGene-small-mn-300x74.png\" alt=\"IntelliGene logo\" width=\"300\" height=\"74\" srcset=\"https:\/\/nesiller.com\/wp-content\/uploads\/2026\/02\/intelliGene-small-mn-300x74.png 300w, https:\/\/nesiller.com\/wp-content\/uploads\/2026\/02\/intelliGene-small-mn-768x190.png 768w, https:\/\/nesiller.com\/wp-content\/uploads\/2026\/02\/intelliGene-small-mn.png 1000w\" sizes=\"(max-width: 300px) 100vw, 300px\" \/><\/p><p class=\"isSelectedEnd\"><strong>IntelliGene Carrier Screening<\/strong> is a genetic test designed to assess an individual&#8217;s risk of passing certain inherited genetic conditions on to their children, even if they do not show any signs or symptoms of the disease. It is particularly recommended for couples planning a pregnancy or during pregnancy to help identify potential genetic risks at an early stage.<\/p><p class=\"isSelectedEnd\">Designed for individuals and couples planning to have healthy children, these genetic tests help identify inherited genetic risks that may be present even in the absence of a family history. They support both carrier screening and infertility assessment, enabling informed reproductive decision-making.<\/p><p>Our carrier screening tests are tailored to each individual&#8217;s personal and family history, ethnic background, and clinical needs.<\/p><p><strong>Our Test Portfolio<\/strong><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/basic-screening-panel\/\"><span style=\"font-weight: 400;\">Intelligene Basic Screening Panel<\/span><\/a><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/comprehensive-panel\/\"><span style=\"font-weight: 400;\">Intelligene Comprehensive Screening Panel<\/span><\/a><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/male-infertility-panel\/\"><span style=\"font-weight: 400;\">Intelligene Male Infertility Panels<\/span><\/a><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/female-infertility-panel\/\"><span style=\"font-weight: 400;\">Intelligene Female Infertility Panels<\/span><\/a><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/sma\/\"><span style=\"font-weight: 400;\">Spinal Muscular Atrophy (SMA)<\/span><\/a><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/cystic-fibrosis-mutation\/\"><span style=\"font-weight: 400;\">Cystic Fibrosis (CFTR)<\/span><\/a><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/fragile-x\/\"><span style=\"font-weight: 400;\">Fragile X Syndrome (FMR1)<\/span><\/a><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/dmd-duchenne-muscular-dystrophy-deletion-duplication-analysis\/\"><span style=\"font-weight: 400;\">Duchenne Muscular Dystrophy (DMD)<\/span><\/a><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/thrombophilia-panel\/\"><span style=\"font-weight: 400;\">Thrombophilia Panel<\/span><\/a><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/y-chromosome-microdeletion\/\"><span style=\"font-weight: 400;\">Y-Chromosome Microdeletion Analysis (YDel)<\/span><\/a><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/phenylketonuria-pku\/\"><span style=\"font-weight: 400;\">Phenylketonuria (PKU)<\/span><\/a><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/thalassemia\/\"><span style=\"font-weight: 400;\">Thalassemia<\/span><\/a><\/li><\/ul><p><span style=\"font-weight: 400;\">Please consult our team regarding <a href=\"https:\/\/nesiller.com\/en\/prenatal-testing\/single-gene-tests\/\">single gene<\/a> disorder analysis not listed above.<\/span><\/p><p class=\"isSelectedEnd\">* Carrier screening enables the assessment of potential genetic risks before pregnancy and, when appropriate, can help guide decisions regarding genetic counseling, prenatal diagnostic options, and assisted reproductive technologies.<\/p><p>** IntelliGene is a registered trademark of Nesiller Genetic Diagnosis and Information Services Inc.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-30d79a1 e-flex e-con-boxed e-con e-parent\" data-id=\"30d79a1\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t<div class=\"elementor-element elementor-element-2bfa030 e-con-full e-flex e-con e-child\" data-id=\"2bfa030\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-62af266 at-heading-animation at-animation-heading-style-3 elementor-widget elementor-widget-heading\" data-id=\"62af266\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;ekit_we_effect_on&quot;:&quot;none&quot;}\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Genetic Counseling<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5c7c787 elementor-invisible elementor-widget elementor-widget-text-editor\" data-id=\"5c7c787\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;_animation&quot;:&quot;fadeInUp&quot;,&quot;_animation_delay&quot;:100,&quot;ekit_we_effect_on&quot;:&quot;none&quot;}\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><b>Laboratory and Process Support<br \/><\/b><b><\/b><span style=\"font-weight: 400;\">Our team provides dedicated guidance at each step of the testing process.<\/span><\/p><p><b>End to End Clinical Support<br \/><\/b><b><\/b><span style=\"font-weight: 400;\">Appropriate test selection and clinical interpretation by Medical Genetics Specialists.<\/span><\/p><p><b>Accessibility<br \/><\/b><b><\/b><span style=\"font-weight: 400;\">Convenient access through both online and in person consultation options.<\/span><\/p><p><b>Dr. G\u00fclay \u00d6zg\u00f6n<br \/><\/b><b>General Manager, Clinical Pharmacology and Medical Geneticist Specialist<\/b><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-039c7fe e-con-full e-flex e-con e-child\" data-id=\"039c7fe\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-2a5b7ef at-image-animation at-animation-image-none at-none elementor-widget elementor-widget-image\" data-id=\"2a5b7ef\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;ekit_we_effect_on&quot;:&quot;none&quot;}\" data-widget_type=\"image.default\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<img fetchpriority=\"high\" decoding=\"async\" width=\"800\" height=\"934\" src=\"https:\/\/nesiller.com\/wp-content\/uploads\/2026\/10\/Dr-Gulay-01-opt.webp\" class=\"attachment-large size-large wp-image-20953\" alt=\"Uzm. Dr. G\u00fclay \u00d6zg\u00f6n\" srcset=\"https:\/\/nesiller.com\/wp-content\/uploads\/2026\/10\/Dr-Gulay-01-opt.webp 800w, https:\/\/nesiller.com\/wp-content\/uploads\/2026\/10\/Dr-Gulay-01-opt-257x300.webp 257w, https:\/\/nesiller.com\/wp-content\/uploads\/2026\/10\/Dr-Gulay-01-opt-768x897.webp 768w\" sizes=\"(max-width: 800px) 100vw, 800px\" \/>\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-9f77dd9 elementor-widget elementor-widget-html\" data-id=\"9f77dd9\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;ekit_we_effect_on&quot;:&quot;none&quot;}\" data-widget_type=\"html.default\">\n\t\t\t\t\t<script type=\"application\/ld+json\">{\"@context\":\"https:\/\/schema.org\",\"@type\":\"Person\",\"@id\":\"https:\/\/nesiller.com\/#gulay-ozgon\",\"name\":\"G\u00fclay \u00d6zg\u00f6n\",\"honorificPrefix\":\"Dr.\",\"jobTitle\":\"General Manager, Clinical Pharmacology and Medical Geneticist Specialist\",\"worksFor\":{\"@id\":\"https:\/\/nesiller.com\/en\/#organization\/\"},\"sameAs\":[\"https:\/\/www.linkedin.com\/in\/gulayozgon\"]}<\/script>\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>IntelliGene Carrier Screening assesses an individual&#8217;s risk of passing inherited genetic conditions to their children even without symptoms, before or during pregnancy, with essential and comprehensive panels plus female and male infertility panels.<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"elementor_header_footer","meta":{"footnotes":""},"class_list":["post-12705","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/pages\/12705","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/comments?post=12705"}],"version-history":[{"count":53,"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/pages\/12705\/revisions"}],"predecessor-version":[{"id":21745,"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/pages\/12705\/revisions\/21745"}],"wp:attachment":[{"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/media?parent=12705"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}