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- 2023
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Mark
Deficiency of the Heterogeneous Nuclear Ribonucleoprotein U locus leads to delayed hindbrain neurogenesis
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- Contribution to journal › Article
- 2020
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Mark
Presynaptic dysfunction in CASK-related neurodevelopmental disorders
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- Contribution to journal › Article
- 2019
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Mark
NRXN1 Deletion and Exposure to Methylmercury Increase Astrocyte Differentiation by Different Notch-Dependent Transcriptional Mechanisms
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- Contribution to journal › Article
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Mark
Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186
(
- Contribution to journal › Article
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Mark
Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality
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- Contribution to journal › Article
- 2014
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Mark
The Roots of Autism and ADHD Twin Study in Sweden (RATSS)
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- Contribution to journal › Article
- 2007
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Mark
Association of adenomatous polyposis coli (APC) gene polymorphisms with autism spectrum disorder (ASD)
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- Contribution to journal › Article
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Mark
Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients
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- Contribution to journal › Article
- 2001
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Mark
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity
(
- Contribution to journal › Article