[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"detail-sidebar-cat-0-en-105":3,"doc-seo-497432-105":59,"doc-detail-497432-en":130},{"code":4,"msg":5,"data":6},0,"success",[7,13,18,23,28,33,38,43,48,51,55],{"id":8,"doc_module":4,"doc_module_name":9,"category_name":10,"show_sort_weight":11,"slug":12},1,"Document","Story & Novel",90,"story-novel",{"id":14,"doc_module":4,"doc_module_name":9,"category_name":15,"show_sort_weight":16,"slug":17},2,"Literature",80,"literature",{"id":19,"doc_module":4,"doc_module_name":9,"category_name":20,"show_sort_weight":21,"slug":22},4,"Exam",70,"exam",{"id":24,"doc_module":4,"doc_module_name":9,"category_name":25,"show_sort_weight":26,"slug":27},5,"Comic",60,"comic",{"id":29,"doc_module":4,"doc_module_name":9,"category_name":30,"show_sort_weight":31,"slug":32},6,"Technology",50,"technology",{"id":34,"doc_module":4,"doc_module_name":9,"category_name":35,"show_sort_weight":36,"slug":37},7,"Healthcare",40,"healthcare",{"id":39,"doc_module":4,"doc_module_name":9,"category_name":40,"show_sort_weight":41,"slug":42},8,"Research & Report",30,"research-report",{"id":44,"doc_module":4,"doc_module_name":9,"category_name":45,"show_sort_weight":46,"slug":47},9,"Religion & Spirituality",20,"religion-spirituality",{"id":46,"doc_module":4,"doc_module_name":9,"category_name":49,"show_sort_weight":46,"slug":50},"World Cup","world-cup",{"id":52,"doc_module":4,"doc_module_name":9,"category_name":53,"show_sort_weight":52,"slug":54},10,"Lifestyle","lifestyle",{"id":56,"doc_module":4,"doc_module_name":9,"category_name":57,"show_sort_weight":24,"slug":58},19,"General","general",{"code":4,"msg":60,"data":61},"ok",{"site_id":62,"language":63,"slug":64,"title":65,"keywords":66,"description":67,"schema_data":68,"social_meta":123,"head_meta":125,"extra_data":127,"updated_unix":129},105,"en","genomics-in-general-practice-whats-new-2023-update","Genomics in general practice - What’s new - 2023 update","","A comprehensive clinical resource on genomics in general practice, covering background, purpose, development process, formatting, and a “What’s new” section. It defines scope and ethical principles, explains clinical genetics and genetic counselling, and discusses genetics support groups, insurance issues, and common misconceptions. The guide surveys core genetic tests and technologies (microarray, newborn screening, personal genomic testing, pharmacogenomics, prenatal and carrier screening) and applies them to family history and disease-specific topics across multiple conditions.",{"@graph":69,"@context":122},[70,84,105],{"@type":71,"itemListElement":72},"BreadcrumbList",[73,77,79,82],{"item":74,"name":75,"@type":76,"position":8},"https://docshare.wps.com","Home","ListItem",{"item":78,"name":9,"@type":76,"position":14},"https://docshare.wps.com/document/",{"item":80,"name":35,"@type":76,"position":81},"https://docshare.wps.com/document/healthcare/",3,{"item":83,"name":65,"@type":76,"position":19},"https://docshare.wps.com/document/genomics-in-general-practice-whats-new-2023-update/497432/",{"url":83,"name":65,"@type":85,"image":86,"author":91,"headline":65,"publisher":94,"fileFormat":97,"inLanguage":63,"description":67,"dateModified":98,"datePublished":99,"encodingFormat":97,"isAccessibleForFree":100,"interactionStatistic":101},"DigitalDocument",{"url":87,"@type":88,"width":89,"height":90},"https://docshare.wps.com/thumbnails/genomics-in-general-practice-whats-new-2023-update/497432.png","ImageObject",300,407,{"name":92,"@type":93},"Đào","Person",{"url":74,"name":95,"@type":96},"DocShare","Organization","application/pdf","2026-11-06","2026-10-02",true,{"@type":102,"interactionType":103,"userInteractionCount":24},"InteractionCounter",{"@type":104},"ViewAction",{"@type":106,"mainEntity":107},"FAQPage",[108,114,118],{"name":109,"@type":110,"acceptedAnswer":111},"What does the resource cover for genomics in general practice?","Question",{"text":112,"@type":113},"It covers background, aims, development process, formatting, updates (“What’s new”), scope, ethical principles, and practical areas including counselling and support resources.","Answer",{"name":115,"@type":110,"acceptedAnswer":116},"Which genetic tests and technologies are included?",{"text":117,"@type":113},"The resource includes chromosome microarray, newborn screening, personal genomic testing, pharmacogenomics, prenatal testing, and reproductive carrier screening.",{"name":119,"@type":110,"acceptedAnswer":120},"How are disease-specific topics organized?",{"text":121,"@type":113},"Disease-specific topics are presented as dedicated sections, including Alzheimer disease, autism spectrum disorder, diabetes, familial cancers, haemoglobinopathies, and other hereditary conditions.","https://schema.org",{"og:url":83,"og:type":124,"og:title":65,"og:site_name":95,"og:description":67},"article",{"robots":126,"canonical":83},"index,follow",{"doc_id":128,"site_id":62},497432,1791244457,{"code":4,"msg":5,"data":131},{"doc_id":128,"user_id":132,"nickname":92,"user_avatar":133,"doc_module":4,"category_id":34,"category_name":35,"doc_title":65,"doc_description":67,"doc_content":134,"file_id":135,"file_url":136,"file_type":137,"file_size":138,"view_count":24,"is_deleted":4,"is_public":8,"is_downloadable":8,"audit_status":8,"page_count":139,"language":140,"language_code":63,"site_id":62,"html_lang":63,"table_of_contents":141,"faqs":142,"seo_title":143,"seo_description":67,"update_tm":144,"read_time":145,"preview_page_count":4},1374402968488,"https://ap-avatar.wpscdn.com/davatar_29158cc5080c5b710cf443261637dec0","Genomics in general practice  \nLast updated: 19 12 2023  \n1. Genomics in general practice ............................................................................................................ 1  \n1. Background .......................................................................................................................... 2  \n2. Aim of the resource ............................................................................................................. 3  \n3. Development process ..........................................................................................................4  \n4. A note on the title of the resource ...................................................................................... 5  \n5. Format .................................................................................................................................. 6  \n6. What’s new ........................................................................................................................... 9  \n7. Scope .................................................................................................................................. 10  \n8. Ethical principles ................................................................................................................ 11  \n9. Clinical Genetics and Genetic Counselling....................................................................... 13  \n10. Genetics support groups and organisations.................................................................... 14  \n11. Health and life insurance issues ....................................................................................... 15  \n12. Misconceptions about genetics........................................................................................ 17  \n2. Genetic tests and technologies ....................................................................................................... 19  \n1. Chromosome microarray...................................................................................................20  \n2. Newborn screening ............................................................................................................23  \n3. Personal genomic testing..................................................................................................27  \n4. Pharmacogenomics...........................................................................................................32  \n5. Prenatal testing ..................................................................................................................37  \n6. Reproductive carrier screening .........................................................................................43  \n3. Family history....................................................................................................................................46  \n4. Disease specific topics .................................................................................................................... 51  \n1. Alzheimer disease.............................................................................................................. 52  \n2. Autism spectrum disorder.................................................................................................54  \n3. Cystic fibrosis ..................................................................................................................... 57  \n4. Developmental delay and intellectual disability ...............................................................60  \n5. Diabetes .............................................................................................................................. 63  \n6. Familial breast and ovarian cancer ...................................................................................65  \n7. Familial colorectal cancer .................................................................................................69  \n8. Familial hypercholes","cbCaiextoI5JsgCl","https://ap.wps.com/l/cbCaiextoI5JsgCl","pdf",716964,129,"English","# Genomics in general practice\n## Background\n## Aim of the resource\n## Development process\n## A note on the title of the resource\n## Format\n## What’s new\n## Scope\n## Ethical principles\n## Clinical Genetics and Genetic Counselling\n## Genetics support groups and organisations\n## Health and life insurance issues\n## Misconceptions about genetics\n# Genetic tests and technologies\n## Chromosome microarray\n## Newborn screening\n## Personal genomic testing\n## Pharmacogenomics\n## Prenatal testing\n## Reproductive carrier screening\n# Family history\n# Disease specific topics\n## Alzheimer disease\n## Autism spectrum disorder\n## Cystic fibrosis\n## Developmental delay and intellectual disability\n## Diabetes\n## Familial breast and ovarian cancer\n## Familial colorectal cancer\n## Familial hypercholesterolaemia\n## Familial melanoma\n## Familial prostate cancer\n## Fragile X syndrome and associated conditions\n## Haemoglobinopathies\n## Hereditary haemochromatosis\n## Hereditary thrombophilia\n## Mental health conditions\n## MTHFR gene testing\n## Neurofibromatosis type 1\n## Neurological conditions\n## Sudden arrhythmic death syndrome\n# Summary of genetic tests\n# Supplementary material\n## Acknowledgements\n## Disclaimer","[{\"question\":\"What does the resource cover for genomics in general practice?\",\"answer\":\"It covers background, aims, development process, formatting, updates (“What’s new”), scope, ethical principles, and practical areas including counselling and support resources.\"},{\"question\":\"Which genetic tests and technologies are included?\",\"answer\":\"The resource includes chromosome microarray, newborn screening, personal genomic testing, pharmacogenomics, prenatal testing, and reproductive carrier screening.\"},{\"question\":\"How are disease-specific topics organized?\",\"answer\":\"Disease-specific topics are presented as dedicated sections, including Alzheimer disease, autism spectrum disorder, diabetes, familial cancers, haemoglobinopathies, and other hereditary conditions.\"}]","Genomics in general practice - What’s new - 2023 update | PDF",1790955602,325]