Parents may prefer prognostic uncertainty about their child's genetic neurodevelopmental condition-Reference-Cited by-同舟云学术

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Parents may prefer prognostic uncertainty about their child's genetic neurodevelopmental condition

Published:2024-01-12 Issue:7 Volume:66 Page:828-829
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:Develop Med Child Neuro

Author:

Tyynismaa Henna¹^ORCID

Affiliation:

1. Department of Medical and Clinical Genetics & Stem Cells and Metabolism Research Program, Faculty of Medicine University of Helsinki Helsinki Finland

Abstract

This commentary is on the original article by Turbitt et al. on pages 872–881 of this issue.

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/dmcn.15853

Reference5 articles.

1. Genetic Testing in Neurodevelopmental Disorders

2. Parents' preferences for receiving and discussing prognostic genetic information regarding their children's neurodevelopmental condition: A qualitative study;Turbitt E;Dev Med Child Neurol.,2024

3. Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants

4. A sensitive and reproducible qRT-PCR assay detects physiological relevant trace levels of FMR1 mRNA in individuals with Fragile X syndrome

5. Epigenetics of fragile X syndrome and fragile X-related disorders

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1. Parental diagnostic delay and developmental outcomes in congenital and childhood‐onset myotonic dystrophy type 1;Developmental Medicine & Child Neurology;2024-09-04

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