Last Posted: Feb 13, 2020
- Association of Genetic Risks With Autism Spectrum Disorder and Early Neurodevelopmental Delays Among Children Without Intellectual Disability.
Takahashi Nagahide et al. JAMA network open 2020 Feb 3(2) e1921644 - Fragile X syndrome: clinical presentation, pathology and treatment.
Salcedo-Arellano María Jimena et al. Gaceta medica de Mexico 2020 156(1) 60-66 - Recent ultra-rare inherited mutations identify novel autism candidate risk genes
AB Wilfert et al, BIORXIV preprints, February 11, 2020 - Cascade Testing for Fragile X Syndrome in a Rural Setting in Cameroon (Sub-Saharan Africa).
Kengne Kamga Karen et al. Genes 2020 Jan 11(2) - Largest-Ever Genetic Study of Autism Yields New Insights
NIH Director Blog, February 2020 - Study of Children with One vs. Two or More Siblings with Autism Spectrum Disorder: Expected and Unexpected Similarities and Differences
RF Green et al, CDC Blog Post, February 4, 2020 - Autism Spectrum Disorders: Prenatal Genetic Testing and Abortion Decision-Making among Taiwanese Mothers of Affected Children.
Chen Wei-Ju et al. International journal of environmental research and public health 2020 Jan 17(2) - The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.
Wayhelova Marketa et al. BMC medical genomics 2019 12(1) 111 - Autism heritability: It probably does not mean what you think it means
B Lee, Spectrum, January 7, 2020 - Biomarkers in autism spectrum disorders: Current progress.
Shen Liming et al. Clinica chimica acta; international journal of clinical chemistry 2019 Dec 50241-54
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