^Diagnostic And Statistical Manual Of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR). 美國: American Psychiatric Association Publishing. 2022-03-18. ISBN 978-0890425763.
^Reynolds CR, Goldstein S. Handbook of neurodevelopmental and genetic disorders in children. New York: The Guilford Press. 1999: 3–8. ISBN 978-1-57230-448-2.
^Morris-Rosendahl, Deborah J.; Crocq, Marc-Antoine. Neurodevelopmental disorders—the history and future of a diagnostic concept. Dialogues in Clinical Neuroscience. March 2020, 22 (1): 65–72. ISSN 1294-8322. PMC 7365295. PMID 32699506. doi:10.31887/DCNS.2020.22.1/macrocq.
^Alzheimer's, ADHD, Autism, Brain Injury Treatment, Mood Disorders New Jersey: The NeuroCognitive and Behavioral Institute » Neurodevelopmental Disorders. [2022-04-25](美国英语).
^Morris-Rosendahl, Deborah J.; Crocq, Marc-Antoine. Neurodevelopmental disorders—the history and future of a diagnostic concept. Dialogues in Clinical Neuroscience. March 2020, 22 (1): 65–72. ISSN 1294-8322. PMC 7365295. PMID 32699506. doi:10.31887/DCNS.2020.22.1/macrocq.
^ 7.07.1. National Association of Down Syndrome. (原始内容存档于2012-04-03).
^Hernan Valdes-Socin, Matilde Rubio Almanza, Mariana Tomé Fernández-Ladreda, et al. Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes.。 Frontiers in Endocrinology 2014, 5: 109. review
^SULKES.STEPHEN. Definition of Developmental Disorders - Children's Health Issues. MSD Manual Consumer Version. 2019-08-22 [2019-08-23].
^Murray RM, Lewis SW. Is schizophrenia a neurodevelopmental disorder?. British Medical Journal. September 1987, 295 (6600): 681–2. PMC 1247717. PMID 3117295. doi:10.1136/bmj.295.6600.681.
^Overlapping Behavioral Characteristics of FASD's & Related Mental Health Diagnosis. www.fasdfamilies.com. Cathy Bruer-Thompson. [28 July 2019].[永久失效連結]
^May, Philip A.; Chambers, Christina D.; Kalburg, Wendy O. Prevalence of Fetal Alcohol Spectrum Disorders in 4 US Communities. JAMA. 2018, 319 (5): 474–482 [28 January 2021]. PMC 5839298. PMID 29411031. doi:10.1001/jama.2017.21896. (原始内容于25 January 2021).
^Mammarella IC, Cornoldi C. Nonverbal learning disability (developmental visuospatial disorder). Handbook of Clinical Neurology. 2020, 174: 83–91. ISBN 9780444641489. PMID 32977898. S2CID 221939377. doi:10.1016/B978-0-444-64148-9.00007-7.
^Mammarella IC, Cornoldi C. An analysis of the criteria used to diagnose children with Nonverbal Learning Disability (NLD). Child Neuropsychology. 2014-05-04, 20 (3): 255–80,256. PMID 23705673. S2CID 34107811. doi:10.1080/09297049.2013.796920. hdl:11577/2668053.
^Morris-Rosendahl, Deborah J.; Crocq, Marc-Antoine. Neurodevelopmental disorders—the history and future of a diagnostic concept. Dialogues in Clinical Neuroscience. 31 March 2020, 22 (1): 65–72. PMC 7365295. PMID 32699506. doi:10.31887/DCNS.2020.22.1/macrocq.
^Pletikos M, Sousa AM, Sedmak G, Meyer KA, Zhu Y, Cheng F, et al. Temporal specification and bilaterality of human neocortical topographic gene expression. Neuron. January 2014, 81 (2): 321–32. PMC 3931000. PMID 24373884. doi:10.1016/j.neuron.2013.11.018.
^Samaco RC, Hogart A, LaSalle JM. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Human Molecular Genetics. February 2005, 14 (4): 483–92. PMC 1224722. PMID 15615769. doi:10.1093/hmg/ddi045.
^van IJzendoorn MH, Palacios J, Sonuga-Barke EJ, Gunnar MR, Vorria P, McCall RB, et al. Children in Institutional Care: Delayed Development and Resilience. Monographs of the Society for Research in Child Development. December 2011, 76 (4): 8–30. PMC 4130248. PMID 25125707. doi:10.1111/j.1540-5834.2011.00626.x.
^Nelson CA, Zeanah CH, Fox NA, Marshall PJ, Smyke AT, Guthrie D. Cognitive recovery in socially deprived young children: the Bucharest Early Intervention Project. Science. December 2007, 318 (5858): 1937–40. Bibcode:2007Sci...318.1937N. PMID 18096809. S2CID 1460630. doi:10.1126/science.1143921.[永久失效連結]
^Diamandopoulos K, Green J. Down syndrome: An integrative review. Journal of Neonatal Nursing. October 2018, 24 (5): 235–241. S2CID 57620027. doi:10.1016/j.jnn.2018.01.001.
^Martin JP, Bell J. A pedigree of mental defect showing sex-linkage. Journal of Neurology and Psychiatry. July 1943, 6 (3–4): 154–7. PMC 1090429. PMID 21611430. doi:10.1136/jnnp.6.3-4.154.
^Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics. October 1999, 23 (2): 185–8. PMID 10508514. S2CID 3350350. doi:10.1038/13810.
^Merla G, Howald C, Henrichsen CN, Lyle R, Wyss C, Zabot MT, et al. Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes. American Journal of Human Genetics. August 2006, 79 (2): 332–41. PMC 1559497. PMID 16826523. doi:10.1086/506371.
^Martin CL, Ledbetter DH. Chromosomal Microarray Testing for Children With Unexplained Neurodevelopmental Disorders. JAMA. June 2017, 317 (24): 2545–2546. PMC 7058144. PMID 28654998. doi:10.1001/jama.2017.7272.