Genotype-phenotype correlations with autism spectrum disorder-related traits in noonan syndrome and noonan syndrome with multiple lentigines: a cross-sectional study.

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Title: Genotype-phenotype correlations with autism spectrum disorder-related traits in noonan syndrome and noonan syndrome with multiple lentigines: a cross-sectional study.
Authors: McGhee CA; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA. camcghee@stanford.edu., Plank JR; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA., Pannone L; Molecular Genetics and Functional Genomics Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.; Department of Oncology and Molecular Medicine, Istituto Superiore Di Sanità, Rome, Italy., Russo O; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA., Fuhrmann N; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA., Ruggeri A; Molecular Genetics and Functional Genomics Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Radio FC; Molecular Genetics and Functional Genomics Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Martinelli S; Department of Oncology and Molecular Medicine, Istituto Superiore Di Sanità, Rome, Italy., Tartaglia M; Molecular Genetics and Functional Genomics Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Green T; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA.
Source: Molecular autism [Mol Autism] 2025 Oct 11; Vol. 16 (1), pp. 51. Date of Electronic Publication: 2025 Oct 11.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101534222 Publication Model: Electronic Cited Medium: Internet ISSN: 2040-2392 (Electronic) NLM ISO Abbreviation: Mol Autism Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:2040-2392
DOI:10.1186/s13229-025-00681-1