{"id":800,"date":"2017-01-04T23:44:11","date_gmt":"2017-01-04T20:14:11","guid":{"rendered":"http:\/\/ebnsinagenelab.com\/?page_id=800"},"modified":"2017-01-07T13:04:50","modified_gmt":"2017-01-07T09:34:50","slug":"%d9%be%d8%a7%d9%86%d9%84-%d8%ba%d8%b1%d8%a8%d8%a7%d9%84%da%af%d8%b1%db%8c-%d9%86%d8%a7%d9%82%d9%84%db%8c%d9%86-%d8%a8%d9%87-%d8%a8%db%8c%d9%85%d8%a7%d8%b1%db%8c%d9%87%d8%a7%db%8c-%d8%b4%d8%a7%db%8c","status":"publish","type":"page","link":"https:\/\/ebnsinagenelab.com\/?page_id=800","title":{"rendered":"\u067e\u0627\u0646\u0644 \u063a\u0631\u0628\u0627\u0644\u06af\u0631\u06cc \u0646\u0627\u0642\u0644\u06cc\u0646 \u0628\u0647 \u0628\u06cc\u0645\u0627\u0631\u06cc\u0647\u0627\u06cc \u0634\u0627\u06cc\u0639 \u062a\u06a9 \u0698\u0646\u06cc"},"content":{"rendered":"

\u067e\u0627\u0646\u0644 \u063a\u0631\u0628\u0627\u0644\u06af\u0631\u06cc \u0646\u0627\u0642\u0644\u06cc\u0646 \u0628\u0647 \u0628\u06cc\u0645\u0627\u0631\u06cc\u0647\u0627\u06cc \u0634\u0627\u06cc\u0639 \u062a\u06a9 \u0698\u0646\u06cc\u00a0<\/span><\/p>\n

( Carrier Screening Panels For Common Monogenic Diseases )<\/span><\/p>\n\n\n\n\n\n\n\n\n\n\n
\u00a0<\/caption>\n
\u06a9\u062f \u0622\u0632\u0645\u0627\u06cc\u0634<\/strong><\/td>\n\u0639\u0646\u0648\u0627\u0646<\/strong><\/td>\n\u062a\u0634\u062e\u06cc\u0635 \u0628\u06cc\u0645\u0627\u0631\u06cc<\/strong><\/td>\n\u0646\u0627\u0645 \u0698\u0646(\u0647\u0627)<\/strong><\/td>\n\u0646\u0645\u0648\u0646\u0647 \u0645\u0648\u0631\u062f \u0646\u06cc\u0627\u0632<\/strong><\/td>\n\u0631\u0648\u0634 \u0622\u0646\u0627\u0644\u06cc\u0632<\/strong><\/td>\n\u0645\u062f\u062a \u0622\u0646\u0627\u0644\u06cc\u0632<\/strong><\/td>\n<\/tr>\n
DX0579<\/td>\nEmbryoSeq\u2010PGD for monogenic diseases and HLA matching<\/td>\n\u067e\u0627\u0646\u0644 \u063a\u0631\u0628\u0627\u0644\u06af\u0631\u06cc \u0646\u0627\u0642\u0644\u06cc\u0646 \u0628\u0647 \u0628\u06cc\u0645\u0627\u0631\u06cc\u0647\u0627\u06cc \u0634\u0627\u06cc\u0639 \u062a\u06a9 \u0698\u0646\u06cc<\/td>\nScreening of embryos before
\nimplantation for monogenic disorders as
\nwell as testing for HLA matching. Please
\nsee test description leaflet or contact us
\nfor more information.<\/td>\n		\u062e\u0648\u0646 \u0648\u0631\u06cc\u062f\u06cc \u062d\u0627\u0648\u06cc EDTA<\/td>\nNGS<\/td>\n\u062f\u0648 \u0645\u0627\u0647<\/td>\n<\/tr>\n
DX0577<\/td>\nEmbryoSeq\u2010PGD for monogenic diseases<\/td>\n\u067e\u0627\u0646\u0644 \u063a\u0631\u0628\u0627\u0644\u06af\u0631\u06cc \u0646\u0627\u0642\u0644\u06cc\u0646 \u0628\u0647 \u0628\u06cc\u0645\u0627\u0631\u06cc\u0647\u0627\u06cc \u0634\u0627\u06cc\u0639 \u062a\u06a9 \u0698\u0646\u06cc<\/td>\nScreening of embryos before
\nimplantation for monogenic disorders.
\nPlease see test description leaflet or
\ncontact us for more information.<\/td>\n		\u062e\u0648\u0646 \u0648\u0631\u06cc\u062f\u06cc \u062d\u0627\u0648\u06cc EDTA<\/td>\nNGS<\/td>\n\u062f\u0648 \u0645\u0627\u0647<\/td>\n<\/tr>\n
DX0556<\/td>\nEmbryoSeq\u2010PGS<\/td>\n\u067e\u0627\u0646\u0644 \u063a\u0631\u0628\u0627\u0644\u06af\u0631\u06cc \u0646\u0627\u0642\u0644\u06cc\u0646 \u0628\u0647 \u0628\u06cc\u0645\u0627\u0631\u06cc\u0647\u0627\u06cc \u0634\u0627\u06cc\u0639 \u062a\u06a9 \u0698\u0646\u06cc<\/td>\nScreening of embryos before
\nimplantation for chromosomal
\nabnormalities. Please see test description
\nleaflet or contact us for more information<\/td>\n		\u062e\u0648\u0646 \u0648\u0631\u06cc\u062f\u06cc \u062d\u0627\u0648\u06cc EDTA<\/td>\nNGS<\/td>\n\u0633\u0647 \u0645\u0627\u0647<\/td>\n<\/tr>\n
DX0023<\/td>\nAngelCare, Newborn Genetic Screening \/ Testing<\/td>\n\u067e\u0627\u0646\u0644 \u063a\u0631\u0628\u0627\u0644\u06af\u0631\u06cc \u0646\u0627\u0642\u0644\u06cc\u0646 \u0628\u0647 \u0628\u06cc\u0645\u0627\u0631\u06cc\u0647\u0627\u06cc \u0634\u0627\u06cc\u0639 \u062a\u06a9 \u0698\u0646\u06cc<\/td>\nTesting for 50 common inherited
\ndisorders plus pharmacogenetic testing
\nfor 20 pediatric drugs. Please see test
\ndescription leaflet or contact us for more
\ninformation.<\/td>\n		\u062e\u0648\u0646 \u0648\u0631\u06cc\u062f\u06cc \u062d\u0627\u0648\u06cc EDTA<\/td>\nNGS<\/td>\n\u06f2-\u06f3 \u0645\u0627\u0647<\/td>\n<\/tr>\n
DX0013<\/td>\nCarrierSeq\u2010\u06f6\u06f0\u06f0: Screening of common mutations for 600 Genetic Diseases (Pre\u2010marriage \/ Preconception screening)<\/td>\n\u067e\u0627\u0646\u0644 \u063a\u0631\u0628\u0627\u0644\u06af\u0631\u06cc \u0646\u0627\u0642\u0644\u06cc\u0646 \u0628\u0647 \u0628\u06cc\u0645\u0627\u0631\u06cc\u0647\u0627\u06cc \u0634\u0627\u06cc\u0639 \u062a\u06a9 \u0698\u0646\u06cc<\/td>\nTesting common mutations associated
\nwith more than 600 genetics disorders
\n(hot spot mutations only) . Please see
\ntest description leaflet or contact us for
\nmore information<\/td>\n		\u062e\u0648\u0646 \u0648\u0631\u06cc\u062f\u06cc \u062d\u0627\u0648\u06cc EDTA<\/td>\nNGS<\/td>\n\u062f\u0648 \u0645\u0627\u0647<\/td>\n<\/tr>\n
DX0010\u2010 \u06f1\u06f3\u06f1<\/td>\nCarrierSeq\u2010\u06f1\u06f3\u06f1: Screening of 131 Common Genetic Diseases (Premarriage \/ Preconception screening):<\/td>\n\u067e\u0627\u0646\u0644 \u063a\u0631\u0628\u0627\u0644\u06af\u0631\u06cc \u0646\u0627\u0642\u0644\u06cc\u0646 \u0628\u0647 \u0628\u06cc\u0645\u0627\u0631\u06cc\u0647\u0627\u06cc \u0634\u0627\u06cc\u0639 \u062a\u06a9 \u0698\u0646\u06cc<\/td>\nPlease see test description leaflets for more information<\/td>\n\u062e\u0648\u0646 \u0648\u0631\u06cc\u062f\u06cc \u062d\u0627\u0648\u06cc EDTA<\/td>\nNGS<\/td>\n\u062f\u0648 \u0645\u0627\u0647<\/td>\n<\/tr>\n
DX0010<\/td>\nCarrierSeq\u2010\u06f1\u06f2: Screening of 12 Common Genetic Diseases (Premarriage \/ Preconception screening): Please see test description leaflets for more information<\/td>\n\u067e\u0627\u0646\u0644 \u063a\u0631\u0628\u0627\u0644\u06af\u0631\u06cc \u0646\u0627\u0642\u0644\u06cc\u0646 \u0628\u0647 \u0628\u06cc\u0645\u0627\u0631\u06cc\u0647\u0627\u06cc \u0634\u0627\u06cc\u0639 \u062a\u06a9 \u0698\u0646\u06cc<\/td>\nDsytrophinopathies (DMD gene),
\nHemophilia A\/B (F8\/F9 genes),
\nAlpha\/Beta Thalassemia
\n(HBA1,HBA2,HBB genes), Sickle\u2010Cell
\nAnemia (HBB gene), Hereditary Hearing
\nLoss and Deafness (GJB2, SLC26A4
\ngenes), Spinal Muscular Atrophy (SMN1
\ngene), Galactosemia (GALT gene),
\nPhenylketonoria (PAH gene), Wilson
\nDisease (ATP7B gene), 21\u2010Hydroylase\u2010
\nDeficient Congenital Adrenal Hyperplasia
\n(CYP2A2 gene), Glycogen Storage Disease
\nType II (GAA gene), Autosomal Recessive
\nPolycystic Disease (PKHD1 gene)<\/td>\n		\u062e\u0648\u0646 \u0648\u0631\u06cc\u062f\u06cc \u062d\u0627\u0648\u06cc EDTA<\/td>\nNGS<\/td>\n\u0633\u0647 \u0645\u0627\u0647<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n","protected":false},"excerpt":{"rendered":"

\u067e\u0627\u0646\u0644 \u063a\u0631\u0628\u0627\u0644\u06af\u0631\u06cc \u0646\u0627\u0642\u0644\u06cc\u0646 \u0628\u0647 \u0628\u06cc\u0645\u0627\u0631\u06cc\u0647\u0627\u06cc \u0634\u0627\u06cc\u0639 \u062a\u06a9 \u0698\u0646\u06cc\u00a0 ( Carrier Screening Panels For Common Monogenic Diseases ) \u00a0 \u06a9\u062f \u0622\u0632\u0645\u0627\u06cc\u0634 \u0639\u0646\u0648\u0627\u0646 \u062a\u0634\u062e\u06cc\u0635 \u0628\u06cc\u0645\u0627\u0631\u06cc \u0646\u0627\u0645 \u0698\u0646(\u0647\u0627) \u0646\u0645\u0648\u0646\u0647 \u0645\u0648\u0631\u062f \u0646\u06cc\u0627\u0632 \u0631\u0648\u0634 \u0622\u0646\u0627\u0644\u06cc\u0632 \u0645\u062f\u062a \u0622\u0646\u0627\u0644\u06cc\u0632 DX0579 EmbryoSeq\u2010PGD for monogenic diseases and HLA matching \u067e\u0627\u0646\u0644 \u063a\u0631\u0628\u0627\u0644\u06af\u0631\u06cc \u0646\u0627\u0642\u0644\u06cc\u0646 \u0628\u0647 \u0628\u06cc\u0645\u0627\u0631\u06cc\u0647\u0627\u06cc \u0634\u0627\u06cc\u0639 \u062a\u06a9 \u0698\u0646\u06cc Screening of embryos before implantation for monogenic […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":747,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"_links":{"self":[{"href":"https:\/\/ebnsinagenelab.com\/index.php?rest_route=\/wp\/v2\/pages\/800"}],"collection":[{"href":"https:\/\/ebnsinagenelab.com\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/ebnsinagenelab.com\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/ebnsinagenelab.com\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/ebnsinagenelab.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=800"}],"version-history":[{"count":16,"href":"https:\/\/ebnsinagenelab.com\/index.php?rest_route=\/wp\/v2\/pages\/800\/revisions"}],"predecessor-version":[{"id":804,"href":"https:\/\/ebnsinagenelab.com\/index.php?rest_route=\/wp\/v2\/pages\/800\/revisions\/804"}],"up":[{"embeddable":true,"href":"https:\/\/ebnsinagenelab.com\/index.php?rest_route=\/wp\/v2\/pages\/747"}],"wp:attachment":[{"href":"https:\/\/ebnsinagenelab.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=800"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}