المؤلفون: Kenneth A. Myers, Ebba Alkhunaizi, Michelle M. Morrow, Jiddeke J.P. van de Kamp, Elysa J. Marco, Suma P. Shankar, Harvey B. Sarnat, Marwan Shinawi, Jacqueline L. Steele, Megan Glassford, Colette P. DeFilippo, Tracy Brandt, Amy Waldman, Houda Zghal Elloumi, Holly Dubbs, Ganka Douglas, Sumit Parikh, Kristin G. Monaghan, Cyril Mignot, David Chitayat, Bénédicte Héron, Linda E. Kim, Farrah Rajabi, Shane C. Quinonez, William D. Graf, Mark C. Hannibal, Aravindhan Veerapandiyan

المساهمون: Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Gastroenterology Endocrinology Metabolism

المصدر: Steele, J L, Morrow, M M, Sarnat, H B, Alkhunaizi, E, Brandt, T, Chitayat, D A, DeFilippo, C P, Douglas, G V, Dubbs, H A, Elloumi, H Z, Glassford, M R, Hannibal, M C, Héron, B, Kim, L E, Marco, E J, Mignot, C, Monaghan, K G, Myers, K A, Parikh, S, Quinonez, S C, Rajabi, F, Shankar, S P, Shinawi, M S, van de Kamp, J J P, Veerapandiyan, A, Waldman, A T & Graf, W D 2022, ' Semaphorin-Plexin Signaling : From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome ', Pediatric Neurology, vol. 126, pp. 65-73 . https://doi.org/10.1016/j.pediatrneurol.2021.10.008Test
Pediatric Neurology, 126, 65-73. Elsevier Inc.

مصطلحات موضوعية: Adult, Male, Adolescent, Autism Spectrum Disorder, X-linked intellectual disability, Genetic counseling, Nerve Tissue Proteins, Receptors, Cell Surface, Semaphorins, Young Adult, Neurodevelopmental disorder, Developmental Neuroscience, Semaphorin, Intellectual Disability, Intellectual disability, Humans, Medicine, Child, Genetic Association Studies, X chromosome, Genetics, biology, business.industry, Plexin, medicine.disease, Neurology, Child, Preschool, Pediatrics, Perinatology and Child Health, biology.protein, Autism, Neurology (clinical), business, Cell Adhesion Molecules, Signal Transduction

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da65a60f3e1ab2780a3d905dd23f1bdfTest
https://doi.org/10.1016/j.pediatrneurol.2021.10.008Test

المؤلفون: Vladimir G. Gainullin, Francisca Millan, Claire Teigen, Julie Scuffins, Andres Moreno-De-Luca, Kevin J. Arvai, H. Lester Kirchner, Matthew T. Oetjens, Houda Zghal Elloumi, Scott M. Myers, Karen E. Wain, Kyle Retterer, Rebecca I. Torene, Christa Lese Martin, Denis R. Pesacreta, David H. Ledbetter

المصدر: JAMA

مصطلحات موضوعية: Adult, Male, Pediatrics, medicine.medical_specialty, Adolescent, Cross-sectional study, 01 natural sciences, Cerebral palsy, 03 medical and health sciences, 0302 clinical medicine, Neurodevelopmental disorder, Interquartile range, Exome Sequencing, medicine, Prevalence, Humans, 030212 general & internal medicine, Genetic Testing, 0101 mathematics, Child, Exome sequencing, Genetic testing, Original Investigation, Retrospective Studies, Asphyxia, medicine.diagnostic_test, business.industry, Cerebral Palsy, 010102 general mathematics, Obstetrics and Gynecology, Genetic Variation, Retrospective cohort study, General Medicine, Middle Aged, medicine.disease, Cross-Sectional Studies, Autism spectrum disorder, Neurodevelopmental Disorders, Child, Preschool, Cohort, Mutation, Female, medicine.symptom, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e21b972c94b43cf08909e42ac0e8f883Test
https://europepmc.org/articles/PMC7856544Test/