The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosis
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference39 articles.
1. The clinical application of genome-wide sequencing for monogenic diseases in Canada: position statement of the Canadian College of Medical Geneticists;Boycott;J. Med. Genet.,2015
2. Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management;Chandler;Genet. Med.,2018
3. Responses to clinical uncertainty in Australian general practice trainees: a cross‐sectional analysis;Cooke;Med. Educ.,2017
4. Impact of variation in practice in the prenatal reporting of variants of uncertain significance by commercial laboratories: need for greater adherence to published guidelines;Cornthwaite;Prenat. Diagn.,2022
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1. Fetal whole genome sequencing as a clinical diagnostic tool: Advantages, limitations and pitfalls;Best Practice & Research Clinical Obstetrics & Gynaecology;2024-12
2. Potentially Missed Diagnoses in Prenatal Versus Postnatal Exome Sequencing in the Lack of Informative Phenotype: Lessons Learned From a Postnatal Cohort;Prenatal Diagnosis;2024-09-05
3. Whole‐genome sequencing: is it appropriate in prenatal setting?;Ultrasound in Obstetrics & Gynecology;2024-05
4. Response to the comment on Diderich et al. “The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosis” (EJMG 66(10),104844);European Journal of Medical Genetics;2024-02
5. Letter to the Editor: Comment to Diderich et al. “The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosis” (EJMG 66(10),104844);European Journal of Medical Genetics;2024-02
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