{"id":7909,"date":"2016-03-24T10:10:29","date_gmt":"2016-03-24T09:10:29","guid":{"rendered":"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molekulargenetische-diagnostik\/"},"modified":"2024-10-07T14:43:54","modified_gmt":"2024-10-07T12:43:54","slug":"molecular-genetics","status":"publish","type":"page","link":"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/","title":{"rendered":"Molecular Genetics"},"content":{"rendered":"
[mk_page_section bg_image=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2016\/07\/LHA0046-wissenschaftlicher-beirat-1900.jpg” bg_position=”center center” bg_repeat=”no-repeat” bg_stretch=”true” min_height=”500″ full_width=”true” section_id=”header-bild” sidebar=”sidebar-1″][vc_column][\/vc_column][\/mk_page_section][mk_page_section sidebar=”sidebar-1″][vc_column][vc_empty_space height=”50px”][vc_column_text align=”center”]\n

Molecular Genetics<\/span><\/h1>\n[\/vc_column_text][vc_empty_space height=”15px”][\/vc_column][\/mk_page_section][mk_page_section min_height=”0″ padding_top=”0″ padding_bottom=”0″ section_id=”anker-1″ sidebar=”sidebar-1″][vc_column width=”3\/4″][vc_column_text]The goal of molecular genetic diagnostics is to confirm or exclude the genetic change that causes a specific condition of interest.<\/p>\n

With next-generation sequencing (NGS) technology we have powerful tools to offer comprehensive analysis at reasonable prices. Depending on the diagnostic question to be answered, we additionally use conventional molecular genetic tests including Sanger sequencing to test for known familial mutations or MLPA (multiplex ligation-dependent probe amplification) to perform gene dosage analysis. If appropriate, we will combine these different analytical methods.<\/p>\n

We will be happy to discuss with you the best possible approach to arrive at a diagnosis in your individual case.[\/vc_column_text][vc_empty_space height=”50px”][\/vc_column][vc_column width=”1\/4″][mk_image src=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2016\/07\/dakks-300×155.jpg” image_width=”300″ image_height=”155″ align=”center”][\/vc_column][\/mk_page_section][vc_row fullwidth=”true” fullwidth_content=”false” css=”.vc_custom_1476440025532{border-top-width: 0px !important;border-right-width: 0px !important;border-bottom-width: 0px !important;background-color: #65dafd !important;border-right-color: #ffffff !important;border-right-style: solid !important;border-top-color: #ffffff !important;border-top-style: solid !important;border-bottom-color: #ffffff !important;border-bottom-style: solid !important;}” el_class=”ankernavigation-light”][vc_column width=”1\/3″ css=”.vc_custom_1476254954470{border-right-width: 1px !important;border-left-width: 2px !important;border-left-color: #ffffff !important;border-left-style: solid !important;border-right-color: #ffffff !important;border-right-style: solid !important;}” el_class=”anker-first”][mk_fancy_title color=”#ffffff” size=”30″ margin_top=”44″ font_family=”none” align=”center”]Disorders<\/a>[\/mk_fancy_title][\/vc_column][vc_column width=”1\/3″ css=”.vc_custom_1476254971139{border-right-width: 2px !important;border-left-width: 1px !important;border-left-color: #ffffff !important;border-left-style: solid !important;border-right-color: #ffffff !important;border-right-style: solid !important;}” el_class=”anker-middle”][mk_fancy_title color=”#ffffff” size=”30″ margin_top=”44″ font_family=”none” align=”center”]Genes<\/a>[\/mk_fancy_title][\/vc_column][vc_column width=”1\/3″ el_class=”anker-last”][mk_fancy_title color=”#ffffff” size=”30″ margin_top=”20″ margin_bottom=”4″ font_family=”none” align=”center”]Forms & Sample Submission<\/a>[\/mk_fancy_title][\/vc_column][\/vc_row][mk_page_section min_height=”0″ padding_top=”0″ padding_bottom=”0″ section_id=”anker-1″ sidebar=”sidebar-1″][vc_column][vc_empty_space height=”100px” el_class=”v-spacer-100″][vc_empty_space el_class=”v-spacer-100″][\/vc_column][\/mk_page_section][mk_page_section][vc_column width=”1\/3″][vc_row_inner][vc_column_inner][vc_empty_space][vc_empty_space][mk_image src=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2015\/12\/left.jpg” image_size=”full” margin_bottom=”0″][vc_empty_space][mk_image src=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2016\/07\/diagnostik-01-287×180-1.jpg” image_size=”full” align=”right” visibility=”hidden-sm” el_class=”padding30t”][\/vc_column_inner][\/vc_row_inner][\/vc_column][vc_column width=”2\/3″][vc_row_inner][vc_column_inner][vc_column_text el_class=”titlebox diagnostik-01″ css=”.vc_custom_1613725453556{margin-bottom: 0px !important;}”]\n

Disorders<\/h2>\n[\/vc_column_text][mk_padding_divider size=”25″ visibility=”visible-sm”][mk_padding_divider visibility=”hidden-sm”][vc_column_text el_class=”padding25lr” css=”.vc_custom_1613725466856{margin-bottom: 0px !important;}”]NGS technology allows parallel sequencing of many genes in a single analysis.<\/p>\n

By selecting a meaningful and appropriate set of genes that are associated with a specific disorder or group of disorders, we increase the chances to find the genetic cause of a given condition timely and at reasonable costs. Based on this approach, we have established a wide range of diagnostic panels.[\/vc_column_text][vc_empty_space][mk_button dimension=”flat” size=”medium” icon=”mk-icon-long-arrow-right” icon_anim=”side” url=”\/erkrankungen” bg_color=”#a6e8fe” btn_hover_bg=”#000000″ text_color=”dark” btn_hover_txt_color=”#ffffff”]learn more[\/mk_button][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/mk_page_section][mk_page_section min_height=”50″ padding_top=”0″ padding_bottom=”0″ sidebar=”sidebar-1″][vc_column][vc_empty_space height=”100px” el_class=”v-spacer-100″][\/vc_column][\/mk_page_section][mk_page_section][vc_column width=”2\/3″][vc_row_inner][vc_column_inner][vc_column_text el_class=”titlebox diagnostik-01″ css=”.vc_custom_1613725477188{margin-bottom: 0px !important;}”]\n

Genes<\/h2>\n[\/vc_column_text][mk_padding_divider visibility=”hidden-sm”][mk_padding_divider size=”25″ visibility=”visible-sm”][vc_column_text el_class=”padding25lr” css=”.vc_custom_1613725486428{margin-bottom: 0px !important;}”]We continually extend our catalogue of genes offered for testing either in a multi-gene panel or as a single-gene analysis. You can directly search our database for the gene you are interested in and learn whether it is offered for analysis.[\/vc_column_text][vc_empty_space][mk_button dimension=”flat” size=”medium” icon=”mk-icon-long-arrow-right” icon_anim=”side” url=”\/gene” bg_color=”#a6e8fe” btn_hover_bg=”#000000″ text_color=”dark” btn_hover_txt_color=”#ffffff”]to search form[\/mk_button][\/vc_column_inner][\/vc_row_inner][\/vc_column][vc_column width=”1\/3″][vc_row_inner][vc_column_inner][vc_empty_space][vc_empty_space][mk_image src=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2016\/07\/content-molekulargen-diagnostik-490×846-1.jpg” image_size=”full” margin_bottom=”0″][vc_empty_space][mk_image src=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2016\/07\/diagnostik-01-287×180-1.jpg” visibility=”hidden-sm”][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/mk_page_section][mk_page_section min_height=”0″ padding_top=”0″ padding_bottom=”0″ section_id=”anker-1″ sidebar=”sidebar-1″][vc_column][vc_empty_space height=”100px” el_class=”v-spacer-100″][\/vc_column][\/mk_page_section][mk_page_section sidebar=”sidebar-1″][vc_column width=”2\/3″][vc_row_inner][vc_column_inner][vc_column_text el_class=”titlebox diagnostik-01″ css=”.vc_custom_1613725515665{margin-bottom: 0px !important;}”]\n

Contact<\/h2>\n[\/vc_column_text][mk_padding_divider visibility=”hidden-sm”][mk_padding_divider size=”25″ visibility=”visible-sm”][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/2″][vc_column_text el_class=”padding25lr” css=”.vc_custom_1613725536972{margin-bottom: 0px !important;}”]\n

Prof. Dr. rer. nat.
\nPeter Burfeind<\/span><\/h4>\n[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”1\/2″][vc_column_text el_class=”padding25lr” css=”.vc_custom_1613725544763{margin-bottom: 0px !important;}”]Tel.: +49-551-39-67595<\/a>
\npeter.burfeind@med.uni-goettingen.de<\/a>[\/vc_column_text][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/2″][vc_column_text el_class=”padding25lr” css=”.vc_custom_1613725552846{margin-bottom: 0px !important;}”]\n

PD Dr. rer. nat.
\nSilke Kaulfu\u00df<\/span><\/h4>\n[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”1\/2″][vc_column_text el_class=”padding25lr” css=”.vc_custom_1613725559394{margin-bottom: 0px !important;}”]Tel.: +49-551-39-69019<\/a>
\nsilke.kaulfuss@med.uni-goettingen.de<\/a>[\/vc_column_text][\/vc_column_inner][\/vc_row_inner][\/vc_column][vc_column width=”1\/3″ offset=”vc_hidden-sm vc_hidden-xs”][vc_row_inner][vc_column_inner][vc_empty_space][vc_empty_space][mk_image src=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2016\/07\/diagnostik-01-287×180-1.jpg” visibility=”hidden-sm”][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/mk_page_section][mk_page_section min_height=”0″ padding_top=”0″ padding_bottom=”0″ sidebar=”sidebar-1″][vc_column][vc_empty_space height=”100px”][\/vc_column][\/mk_page_section]\n<\/div>","protected":false},"excerpt":{"rendered":"

[mk_page_section bg_image=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2016\/07\/LHA0046-wissenschaftlicher-beirat-1900.jpg” bg_position=”center center” bg_repeat=”no-repeat” bg_stretch=”true” min_height=”500″ full_width=”true” section_id=”header-bild” sidebar=”sidebar-1″][vc_column][\/vc_column][\/mk_page_section][mk_page_section sidebar=”sidebar-1″][vc_column][vc_empty_space height=”50px”][vc_column_text align=”center”] Molecular Genetics [\/vc_column_text][vc_empty_space height=”15px”][\/vc_column][\/mk_page_section][mk_page_section min_height=”0″ padding_top=”0″ padding_bottom=”0″ section_id=”anker-1″ sidebar=”sidebar-1″][vc_column width=”3\/4″][vc_column_text]The goal of molecular genetic diagnostics is to confirm or exclude the genetic change that causes a specific condition of interest. With next-generation sequencing (NGS) technology we have powerful tools to offer comprehensive […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":7667,"menu_order":1,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-7909","page","type-page","status-publish","hentry"],"yoast_head":"\nMolecular Genetics - Institut f\u00fcr Humangenetik<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Molecular Genetics - Institut f\u00fcr Humangenetik\" \/>\n<meta property=\"og:description\" content=\"[mk_page_section bg_image=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2016\/07\/LHA0046-wissenschaftlicher-beirat-1900.jpg” bg_position=”center center” bg_repeat=”no-repeat” bg_stretch=”true” min_height=”500″ full_width=”true” section_id=”header-bild” sidebar=”sidebar-1″][vc_column][\/vc_column][\/mk_page_section][mk_page_section sidebar=”sidebar-1″][vc_column][vc_empty_space height=”50px”][vc_column_text align=”center”] Molecular Genetics [\/vc_column_text][vc_empty_space height=”15px”][\/vc_column][\/mk_page_section][mk_page_section min_height=”0″ padding_top=”0″ padding_bottom=”0″ section_id=”anker-1″ sidebar=”sidebar-1″][vc_column width=”3\/4″][vc_column_text]The goal of molecular genetic diagnostics is to confirm or exclude the genetic change that causes a specific condition of interest. With next-generation sequencing (NGS) technology we have powerful tools to offer comprehensive […]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/\" \/>\n<meta property=\"og:site_name\" content=\"Institut f\u00fcr Humangenetik\" \/>\n<meta property=\"article:modified_time\" content=\"2024-10-07T12:43:54+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"3 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/\",\"url\":\"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/\",\"name\":\"Molecular Genetics - Institut f\u00fcr Humangenetik\",\"isPartOf\":{\"@id\":\"https:\/\/www.humangenetik-umg.de\/en\/#website\"},\"datePublished\":\"2016-03-24T09:10:29+00:00\",\"dateModified\":\"2024-10-07T12:43:54+00:00\",\"breadcrumb\":{\"@id\":\"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/www.humangenetik-umg.de\/en\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Genetic Testing\",\"item\":\"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"Molecular Genetics\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/www.humangenetik-umg.de\/en\/#website\",\"url\":\"https:\/\/www.humangenetik-umg.de\/en\/\",\"name\":\"Institut f\u00fcr Humangenetik\",\"description\":\"Institut f\u00fcr Humangenetik der Universit\u00e4tsmedizin G\u00f6ttingen\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/www.humangenetik-umg.de\/en\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Molecular Genetics - Institut f\u00fcr Humangenetik","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/","og_locale":"en_US","og_type":"article","og_title":"Molecular Genetics - Institut f\u00fcr Humangenetik","og_description":"[mk_page_section bg_image=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2016\/07\/LHA0046-wissenschaftlicher-beirat-1900.jpg” bg_position=”center center” bg_repeat=”no-repeat” bg_stretch=”true” min_height=”500″ full_width=”true” section_id=”header-bild” sidebar=”sidebar-1″][vc_column][\/vc_column][\/mk_page_section][mk_page_section sidebar=”sidebar-1″][vc_column][vc_empty_space height=”50px”][vc_column_text align=”center”] Molecular Genetics [\/vc_column_text][vc_empty_space height=”15px”][\/vc_column][\/mk_page_section][mk_page_section min_height=”0″ padding_top=”0″ padding_bottom=”0″ section_id=”anker-1″ sidebar=”sidebar-1″][vc_column width=”3\/4″][vc_column_text]The goal of molecular genetic diagnostics is to confirm or exclude the genetic change that causes a specific condition of interest. With next-generation sequencing (NGS) technology we have powerful tools to offer comprehensive […]","og_url":"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/","og_site_name":"Institut f\u00fcr Humangenetik","article_modified_time":"2024-10-07T12:43:54+00:00","twitter_card":"summary_large_image","twitter_misc":{"Est. reading time":"3 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/","url":"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/","name":"Molecular Genetics - Institut f\u00fcr Humangenetik","isPartOf":{"@id":"https:\/\/www.humangenetik-umg.de\/en\/#website"},"datePublished":"2016-03-24T09:10:29+00:00","dateModified":"2024-10-07T12:43:54+00:00","breadcrumb":{"@id":"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/molecular-genetics\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.humangenetik-umg.de\/en\/"},{"@type":"ListItem","position":2,"name":"Genetic Testing","item":"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/"},{"@type":"ListItem","position":3,"name":"Molecular Genetics"}]},{"@type":"WebSite","@id":"https:\/\/www.humangenetik-umg.de\/en\/#website","url":"https:\/\/www.humangenetik-umg.de\/en\/","name":"Institut f\u00fcr Humangenetik","description":"Institut f\u00fcr Humangenetik der Universit\u00e4tsmedizin G\u00f6ttingen","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.humangenetik-umg.de\/en\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"}]}},"_links":{"self":[{"href":"https:\/\/www.humangenetik-umg.de\/en\/wp-json\/wp\/v2\/pages\/7909","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.humangenetik-umg.de\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.humangenetik-umg.de\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.humangenetik-umg.de\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.humangenetik-umg.de\/en\/wp-json\/wp\/v2\/comments?post=7909"}],"version-history":[{"count":0,"href":"https:\/\/www.humangenetik-umg.de\/en\/wp-json\/wp\/v2\/pages\/7909\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/www.humangenetik-umg.de\/en\/wp-json\/wp\/v2\/pages\/7667"}],"wp:attachment":[{"href":"https:\/\/www.humangenetik-umg.de\/en\/wp-json\/wp\/v2\/media?parent=7909"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}