{"product_id":"cma-750k-with-clinical-exome-sequencing-with-mcc","title":"CMA 750K with Clinical Exome Sequencing With MCC","description":"\u003cp\u003eAmniotic Fluid\/ Chorionic Villus Sample\/Peripheral Venous Blood\/Cord blood,\/Extracted DNA\/Dry Blood Spot\/POC\u003c\/p\u003e\n\u003cdiv class=\"qMYqUG_convSearchResultHighlightRoot\"\u003e\n\u003cdiv class=\"\" data-turn-id-container=\"request-WEB:073b50d4-25d5-4643-ad97-abcdf5ee9a4a-0\" data-is-intersecting=\"true\"\u003e\n\u003csection class=\"text-token-text-primary w-full focus:outline-none has-data-writing-block:pointer-events-none [\u0026amp;:has([data-writing-block])\u0026gt;*]:pointer-events-auto R6Vx5W_threadScrollVars scroll-mb-[calc(var(--scroll-root-safe-area-inset-bottom,0px)+var(--thread-response-height))] scroll-mt-[calc(var(--header-height)+min(200px,max(70px,20svh)))]\" dir=\"auto\" data-turn-id=\"request-WEB:073b50d4-25d5-4643-ad97-abcdf5ee9a4a-0\" data-turn-id-container=\"request-WEB:073b50d4-25d5-4643-ad97-abcdf5ee9a4a-0\" data-testid=\"conversation-turn-2\" data-scroll-anchor=\"false\" data-turn=\"assistant\"\u003e\n\u003cdiv class=\"text-base my-auto mx-auto pb-10 [--thread-content-margin:var(--thread-content-margin-xs,calc(var(--spacing)*4))] @w-sm\/main:[--thread-content-margin:var(--thread-content-margin-sm,calc(var(--spacing)*6))] @w-lg\/main:[--thread-content-margin:var(--thread-content-margin-lg,calc(var(--spacing)*16))] px-(--thread-content-margin)\"\u003e\n\u003cdiv class=\"[--thread-content-max-width:40rem] @w-lg\/main:[--thread-content-max-width:48rem] mx-auto max-w-(--thread-content-max-width) flex-1 group\/turn-messages focus-visible:outline-hidden relative flex w-full min-w-0 flex-col agent-turn\"\u003e\n\u003cdiv class=\"flex max-w-full flex-col gap-4 grow\"\u003e\n\u003cdiv data-message-author-role=\"assistant\" data-message-id=\"1ea932f5-cda9-40c1-bacd-91b9e3754cb0\" data-turn-start-message=\"true\" dir=\"auto\" data-message-model-slug=\"gpt-5-5\" class=\"min-h-8 text-message relative flex w-full flex-col items-end gap-2 text-start break-words whitespace-normal outline-none keyboard-focused:focus-ring [.text-message+\u0026amp;]:mt-1\" tabindex=\"0\"\u003e\n\u003cdiv class=\"flex w-full flex-col gap-1 empty:hidden\"\u003e\n\u003cdiv class=\"markdown prose dark:prose-invert wrap-break-word w-full light markdown-new-styling\"\u003e\n\u003ch3 data-section-id=\"1d3nvra\" data-start=\"0\" data-end=\"58\"\u003eCMA 750K with Clinical Exome Sequencing (CES) with MCC\u003c\/h3\u003e\n\u003cp data-start=\"60\" data-end=\"180\"\u003e\u003cstrong data-start=\"60\" data-end=\"78\"\u003eTest Overview:\u003c\/strong\u003e\u003cbr\u003eCMA 750K with Clinical Exome Sequencing (CES) with MCC is a comprehensive genetic test that combines:\u003c\/p\u003e\n\u003col data-start=\"182\" data-end=\"888\"\u003e\n\u003cli data-section-id=\"11mu8at\" data-start=\"182\" data-end=\"407\"\u003e\n\u003cstrong data-start=\"185\" data-end=\"231\"\u003eChromosomal Microarray Analysis (CMA 750K)\u003c\/strong\u003e – Detects chromosomal deletions, duplications, aneuploidies, regions of homozygosity, and other copy number variations across the genome. \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\n\u003c\/li\u003e\n\u003cli data-section-id=\"dx2bkh\" data-start=\"408\" data-end=\"641\"\u003e\n\u003cstrong data-start=\"411\" data-end=\"446\"\u003eClinical Exome Sequencing (CES)\u003c\/strong\u003e – Analyzes the protein-coding regions (exons) of clinically relevant genes to identify disease-causing genetic variants associated with inherited disorders. \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\n\u003c\/li\u003e\n\u003cli data-section-id=\"13zxij6\" data-start=\"642\" data-end=\"888\"\u003e\n\u003cstrong data-start=\"645\" data-end=\"691\"\u003eMCC (Maternal Cell Contamination Analysis)\u003c\/strong\u003e – Evaluates prenatal samples to determine whether maternal cells are present in the fetal specimen, helping ensure accurate interpretation of genetic results. \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003ch3 data-section-id=\"1nc6tfk\" data-start=\"890\" data-end=\"915\"\u003eClinical Applications\u003c\/h3\u003e\n\u003cul data-start=\"916\" data-end=\"1228\"\u003e\n\u003cli data-section-id=\"18t6dqg\" data-start=\"916\" data-end=\"965\"\u003eDevelopmental delay and intellectual disability\u003c\/li\u003e\n\u003cli data-section-id=\"nj60mf\" data-start=\"966\" data-end=\"993\"\u003eAutism spectrum disorders\u003c\/li\u003e\n\u003cli data-section-id=\"1ibto9\" data-start=\"994\" data-end=\"1025\"\u003eMultiple congenital anomalies\u003c\/li\u003e\n\u003cli data-section-id=\"s5lo7q\" data-start=\"1026\" data-end=\"1062\"\u003eUnexplained neurological disorders\u003c\/li\u003e\n\u003cli data-section-id=\"15ot4nj\" data-start=\"1063\" data-end=\"1092\"\u003eSuspected genetic syndromes\u003c\/li\u003e\n\u003cli data-section-id=\"xezo9n\" data-start=\"1093\" data-end=\"1136\"\u003ePrenatal diagnosis of fetal abnormalities\u003c\/li\u003e\n\u003cli data-section-id=\"hkg0x8\" data-start=\"1137\" data-end=\"1228\"\u003eCases where routine genetic testing is inconclusive \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"11twy89\" data-start=\"1230\" data-end=\"1249\"\u003eSample Required\u003c\/h3\u003e\n\u003cul data-start=\"1250\" data-end=\"1404\"\u003e\n\u003cli data-section-id=\"w826d7\" data-start=\"1250\" data-end=\"1275\"\u003ePeripheral blood (EDTA)\u003c\/li\u003e\n\u003cli data-section-id=\"1urjby8\" data-start=\"1276\" data-end=\"1292\"\u003eAmniotic fluid\u003c\/li\u003e\n\u003cli data-section-id=\"1et95c1\" data-start=\"1293\" data-end=\"1326\"\u003eChorionic Villus Sampling (CVS)\u003c\/li\u003e\n\u003cli data-section-id=\"cndtc\" data-start=\"1327\" data-end=\"1404\"\u003eGenomic DNA (depending on indication) \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"1l3n95q\" data-start=\"1406\" data-end=\"1420\"\u003eAdvantages\u003c\/h3\u003e\n\u003cul data-start=\"1421\" data-end=\"1767\"\u003e\n\u003cli data-section-id=\"1u7n136\" data-start=\"1421\" data-end=\"1523\"\u003eDetects both large chromosomal abnormalities and single-gene mutations in a single testing strategy.\u003c\/li\u003e\n\u003cli data-section-id=\"fw0j8m\" data-start=\"1524\" data-end=\"1594\"\u003eHigher diagnostic yield compared to standalone CMA or exome testing.\u003c\/li\u003e\n\u003cli data-section-id=\"1523r8e\" data-start=\"1595\" data-end=\"1651\"\u003eUseful for complex and undiagnosed genetic conditions.\u003c\/li\u003e\n\u003cli data-section-id=\"1fpe6x9\" data-start=\"1652\" data-end=\"1767\"\u003eProvides comprehensive genomic evaluation for prenatal and postnatal cases. \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"owkoul\" data-start=\"1769\" data-end=\"1788\"\u003eTurnaround Time\u003c\/h3\u003e\n\u003cp data-start=\"1789\" data-end=\"1907\"\u003eTypically \u003cstrong data-start=\"1799\" data-end=\"1812\"\u003e2–6 weeks\u003c\/strong\u003e, depending on the laboratory and complexity of analysis. \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/section\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"Lifecell Diagnostics","offers":[{"title":"Default Title","offer_id":44007229522055,"sku":null,"price":30800.0,"currency_code":"INR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0691\/4241\/3447\/files\/d7b90a2e-954b-4e65-acda-0629646bc049.png?v=1780383562","url":"https:\/\/ourdermastore.com\/products\/cma-750k-with-clinical-exome-sequencing-with-mcc","provider":"Ourdermastore ","version":"1.0","type":"link"}