{"id":7667,"date":"2016-07-25T17:00:30","date_gmt":"2016-07-25T15:00:30","guid":{"rendered":"https:\/\/www.humangenetik-umg.de\/en\/diagnostik\/"},"modified":"2022-04-11T12:54:52","modified_gmt":"2022-04-11T10:54:52","slug":"genetic-testing","status":"publish","type":"page","link":"https:\/\/www.humangenetik-umg.de\/en\/genetic-testing\/","title":{"rendered":"Genetic Testing"},"content":{"rendered":"
[mk_page_section bg_image=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2016\/07\/LHA9813-diagnostik-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

Genetic Testing
\n<\/span><\/h1>\n[\/vc_column_text][vc_empty_space height=”15px”][vc_row_inner is_fullwidth_content=”false”][vc_column_inner width=”3\/4″][vc_column_text]In our genetic diagnostics laboratory, we perform molecular genetic, molecular cytogenetic and cytogenetic testing, using state-of-the-art high-throughput (next-generation) sequencing technology in disease-specific gene panels along with MLPA analysis, array CGH and conventional karyotyping.<\/p>\n

Our services are offered in collaboration with “Medizinisches Versorgungszentrum der UMG Bereich Humangenetik\u201c. All analytical and processing steps in our diagnostic lab are performed under controlled and monitored conditions. We have received accreditation by the German Accreditation Body (DAkkS) in accordance with DIN EN ISO 15189:2014 within the scope of \u201cMedical Laboratory Services\u201d for the areas of \u201cMolecular Human Genetics\u201d and \u201cCytogenetics\u201d.<\/p>\n

We are dedicated to use the latest findings made by our researchers in their various activities to directly support, improve and further develop our routine diagnostic services. This allows us to continually expand our range of tests and to offer genetic diagnostics on the highest technical level and reflecting the latest scientific knowledge.[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_empty_space][vc_empty_space][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” margin_bottom=”20″][\/vc_column_inner][\/vc_row_inner][mk_padding_divider size=”80″][\/vc_column][\/mk_page_section][vc_row fullwidth=”true” fullwidth_content=”false” css=”.vc_custom_1476437534206{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″ el_class=”anker-first”][mk_fancy_title color=”#ffffff” size=”30″ margin_top=”29″ margin_bottom=”19″ font_family=”none” align=”center” animation=”scale-up”]Molecular Genetics<\/a>[\/mk_fancy_title][\/vc_column][vc_column width=”1\/3″ el_class=”anker-middle”][mk_fancy_title color=”#ffffff” size=”30″ margin_top=”29″ margin_bottom=”19″ font_family=”none” align=”center” animation=”scale-up”]Cytogenetics<\/a>[\/mk_fancy_title][\/vc_column][vc_column width=”1\/3″ el_class=”anker-last”][mk_fancy_title color=”#ffffff” size=”30″ margin_top=”28″ font_family=”none” align=”center” animation=”scale-up”]Molecular Cytogenetics<\/a>[\/mk_fancy_title][\/vc_column][\/vc_row][mk_page_section min_height=”0″ padding_top=”0″ padding_bottom=”0″ section_id=”molekulargenetische-diagnostik” sidebar=”sidebar-1″][vc_column][mk_padding_divider visibility=”hidden-sm”][\/vc_column][\/mk_page_section][vc_row fullwidth=”true” fullwidth_content=”false” css=”.vc_custom_1476437534206{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 el_class=”anker-first”][mk_fancy_title color=”#ffffff” size=”30″ margin_top=”29″ margin_bottom=”19″ font_family=”none” align=”center” animation=”scale-up”]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=”molekulargenetische-diagnostik” sidebar=”sidebar-1″][vc_column][vc_empty_space height=”100px”][\/vc_column][\/mk_page_section][mk_page_section section_id=”molekulargenetische diagnostik” sidebar=”sidebar-1″][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”][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 css=”.vc_custom_1470000316929{padding-right: 10px !important;padding-left: 10px !important;}”][vc_column_inner][vc_column_text el_class=”titlebox diagnostik-01″ css=”.vc_custom_1613653465310{margin-bottom: 0px !important;}”]\n

Molecular Genetics<\/h2>\n

<\/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_1613653510974{margin-bottom: 0px !important;}”]The goal of molecular genetic testing is to either 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.[\/vc_column_text][vc_empty_space][mk_button dimension=”flat” size=”medium” icon=”mk-icon-long-arrow-right” icon_anim=”side” url=”\/en\/genetic-testing\/molecular-genetics” 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 section_id=”zytogenetische-diagnostik” sidebar=”sidebar-1″][vc_column][vc_empty_space height=”100px” el_class=”v-spacer-100″][\/vc_column][\/mk_page_section][mk_page_section section_id=”zytogenetische-diagnostik” sidebar=”sidebar-1″][vc_column width=”2\/3″][vc_row_inner css=”.vc_custom_1470000341511{padding-right: 10px !important;padding-left: 10px !important;}”][vc_column_inner][vc_column_text el_class=”titlebox diagnostik-02″ css=”.vc_custom_1613653522333{margin-bottom: 0px !important;}”]\n

Cytogenetics<\/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_1613653531996{margin-bottom: 0px !important;}”]In classical cytogenetic diagnostics, we investigate chromosomes under the light microscope for changes that affect either their number (aneuploidies) or their structure (e.g. inversions, translocations, duplications or deletions).<\/p>\n

This conventional method of chromosome analysis continues to be a useful tool for various indications and is applied for prenatal or postnatal diagnostics.[\/vc_column_text][vc_empty_space][mk_button dimension=”flat” size=”medium” icon=”mk-icon-long-arrow-right” icon_anim=”side” url=”\/en\/genetic-testing\/cytogenetics” bg_color=”#66ccff” btn_hover_bg=”#000000″ text_color=”dark” btn_hover_txt_color=”#ffffff”]learn more[\/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\/contentbilder-zytogen-diagnostik-490×846.jpg” image_size=”full” margin_bottom=”0″][vc_empty_space][mk_image src=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2016\/07\/180×287.jpg” image_size=”full” visibility=”hidden-sm” el_class=”padding30t”][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/mk_page_section][mk_page_section section_id=”molekularzytogenetische-diagnostik” sidebar=”sidebar-1″][vc_column][vc_empty_space height=”100px” el_class=”v-spacer-100″][\/vc_column][\/mk_page_section][mk_page_section section_id=”molekularzytogenetische-diagnostik” sidebar=”sidebar-1″][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\/contentbilder-molekularzytogen-diagnostik-490×846.jpg” image_size=”full” margin_bottom=”0″][vc_empty_space][mk_image src=”https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2016\/10\/diagnostik-03-287×180.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 css=”.vc_custom_1470000355654{padding-right: 10px !important;padding-left: 10px !important;}”][vc_column_inner][vc_column_text el_class=”titlebox diagnostik-03″ css=”.vc_custom_1613653565836{margin-bottom: 0px !important;}”]\n

Molecular Cytogenetics<\/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_1613653597959{margin-bottom: 0px !important;}”]With high-resolution molecular cytogenetic methods, we can detect structural chromosomal changes that are too small to be visible with a light microscope in conventional karyotyping.<\/p>\n

We use array CGH (array-based comparative genomic hybridization) analysis to search at the whole-genome level for submicroscopic chromosome aberrations such as microdeletions or duplications.[\/vc_column_text][vc_empty_space][mk_button dimension=”flat” size=”medium” icon=”mk-icon-long-arrow-right” icon_anim=”side” url=”\/en\/genetic-testing\/molecular-cytogenetics” 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=”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\/LHA9813-diagnostik-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”] Genetic Testing [\/vc_column_text][vc_empty_space height=”15px”][vc_row_inner is_fullwidth_content=”false”][vc_column_inner width=”3\/4″][vc_column_text]In our genetic diagnostics laboratory, we perform molecular genetic, molecular cytogenetic and cytogenetic testing, using state-of-the-art high-throughput (next-generation) sequencing technology in disease-specific gene panels along with MLPA analysis, array CGH and conventional karyotyping. Our services are offered […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-7667","page","type-page","status-publish","hentry"],"yoast_head":"\nGenetic Testing - 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\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Genetic Testing - 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\/LHA9813-diagnostik-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”] Genetic Testing [\/vc_column_text][vc_empty_space height=”15px”][vc_row_inner is_fullwidth_content=”false”][vc_column_inner width=”3\/4″][vc_column_text]In our genetic diagnostics laboratory, we perform molecular genetic, molecular cytogenetic and cytogenetic testing, using state-of-the-art high-throughput (next-generation) sequencing technology in disease-specific gene panels along with MLPA analysis, array CGH and conventional karyotyping. 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