Genomics and Precision Health Database

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Query Trace: Prenatal testing[original query]>>Evidence Synthesis[Product Type]

Publication
Application of exome sequencing for prenatal diagnosis: a rapid scoping review. Pratt Misty et al. Genetics in medicine : official journal of the American College of Medical Genetics 2020 Aug Similar articles in PubMed
Psychosocial implications of living with familial risk of a psychiatric disorder and attitudes to psychiatric genetic testing: A systematic review of the literature. Meiser Bettina et al. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2020 May Similar articles in PubMed
The role of information provision in economic evaluations of non-invasive prenatal testing: a systematic review. John Nikita M et al. The European journal of health economics : HEPAC : health economics in prevention and care 2019 Nov 20(8) 1123-1131 Similar articles in PubMed
Causes of aberrant non-invasive prenatal testing for aneuploidy: A systematic review. Samura Osamu et al. Taiwanese journal of obstetrics & gynecology 2020 Jan 59(1) 16-20 Similar articles in PubMed
Causes of aberrant non-invasive prenatal testing for aneuploidy: A systematic review. Samura Osamu et al. Taiwanese journal of obstetrics & gynecology 2020 Jan 59(1) 16-20 Similar articles in PubMed
Causes of aberrant non-invasive prenatal testing for aneuploidy: A systematic review. Samura Osamu et al. Taiwanese journal of obstetrics & gynecology 2020 Jan 59(1) 16-20 Similar articles in PubMed
Causes of aberrant non-invasive prenatal testing for aneuploidy: A systematic review. Samura Osamu et al. Taiwanese journal of obstetrics & gynecology 2020 Jan 59(1) 16-20 Similar articles in PubMed
Cost-effectiveness of prenatal screening and diagnostic strategies for Down syndrome: A microsimulation modeling analysis. Zhang Wei et al. PloS one 2019 14(12) e0225281 Similar articles in PubMed
Psychological and social consequences of non-invasive prenatal testing (NIPT): a scoping review. Labonté Valérie et al. BMC pregnancy and childbirth 2019 Oct 19(1) 385 Similar articles in PubMed
Prenatal genetic testing for cystic fibrosis: a systematic review of clinical effectiveness and an ethics review. Kessels Sharon J M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Aug Similar articles in PubMed
CLINGEN Actionability Report for Familial Adenomatous Polyposis - APC ClinGen Actionability Working Group
CLINGEN Actionability Report for Factor V Leiden, Homozygous (also includes compound heterozygous FVL + prothrombin G20210A) - F5 ClinGen Actionability Working Group
CLINGEN Actionability Report for Hereditary Hemorrhagic Telangiectasia - ENG, ACVRL1, SMAD4, GDF2 ClinGen Actionability Working Group
CLINGEN Actionability Report for Phenylketonuria (PKU) - PAH ClinGen Actionability Working Group
CLINGEN Actionability Report for Malignant Hyperthermia Susceptibility - RYR1, CACNA1S ClinGen Actionability Working Group
CLINGEN Actionability Report for MUTYH-Associated Polyposis - MUTYH ClinGen Actionability Working Group
CLINGEN Actionability Report for Basal Cell Nevus Syndrome (BCNS) - PTCH1 ClinGen Actionability Working Group
CLINGEN Actionability Report for Multiple Endocrine Neoplasia Type I - MEN1 ClinGen Actionability Working Group
CLINGEN Actionability Report for Hypophosphatemic rickets, autosomal dominant-FGF23 ClinGen Actionability Working Group
CLINGEN Actionability Report for Acrodermatitis enteropathica, zinc-deficiency type-SLC39A4 ClinGen Actionability Working Group
CLINGEN Actionability Report for Homocystinuria due to Cystathionine Beta-Synthase Deficiency - CBS ClinGen Actionability Working Group
CLINGEN Actionability Report for Glycogen Storage Disease 2 - GAA ClinGen Actionability Working Group
CLINGEN Actionability Report for Wilms tumor-WT1 ClinGen Actionability Working Group
CLINGEN Actionability Report for Ehlers-Danlos syndrome, classic type - COL5A1, COL5A2 ClinGen Actionability Working Group
CLINGEN Actionability Report for Pancreatic cancer/melanoma syndrome - CDKN2A ClinGen Actionability Working Group
CLINGEN Actionability Report for Multiple Endocrine Neoplasia IIA, Familial Medullary Thyroid Cancer - RET ClinGen Actionability Working Group
CLINGEN Actionability Report for Juvenile polyposis syndrome - SMAD4, BMPR1A ClinGen Actionability Working Group
CLINGEN Actionability Report for Homozygous Familial Hypercholesterolemia - LDLR, APOB, PCSK9 ClinGen Actionability Working Group
CLINGEN Actionability Report for Familial Hypertrophic Cardiomyopathy - ACTC1, CSRP3, MYBPC3, MYH7, MYL2, MYL3, PRKAG2, TNNI3, TNNT2, TPM1 ClinGen Actionability Working Group
CLINGEN Actionability Report for DICER1-Related Disorders-DICER1 ClinGen Actionability Working Group