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1. A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency. (January 2018)

2. Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome. (22nd November 2019)

3. Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype–phenotype relationships and overlap with Costello syndrome. Issue 12 (17th August 2007)

4. CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Issue 1 (December 2018)

5. Cover Image, Volume 39, Issue 1. Issue 1 (7th December 2017)

6. CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity. (26th May 2021)

7. Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic‐dyskinetic encephalopathy. Issue 7 (6th April 2020)

8. DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome. Issue 1 (11th November 2017)

9. De novo heterozygous missense and loss‐of‐function variants in CDC42BPB are associated with a neurodevelopmental phenotype. Issue 5 (7th February 2020)

10. Defining the phenotypic spectrum of SLC6A1 mutations. (8th January 2018)