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Prenatal diagnosis of hereditary disorders.
Miles JH, Kaback MM. Miles JH, et al. Pediatr Clin North Am. 1978 Aug;25(3):593-618. doi: 10.1016/s0031-3955(16)33606-9. Pediatr Clin North Am. 1978. PMID: 358110 Review. No abstract available.
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder.
Chan AJS, Engchuan W, Reuter MS, Wang Z, Thiruvahindrapuram B, Trost B, Nalpathamkalam T, Negrijn C, Lamoureux S, Pellecchia G, Patel RV, Sung WWL, MacDonald JR, Howe JL, Vorstman J, Sondheimer N, Takahashi N, Miles JH, Anagnostou E, Tammimies K, Zarrei M, Merico D, Stavropoulos DJ, Yuen RKC, Fernandez BA, Scherer SW. Chan AJS, et al. Among authors: miles jh. Nat Commun. 2022 Oct 29;13(1):6463. doi: 10.1038/s41467-022-34112-z. Nat Commun. 2022. PMID: 36309498 Free PMC article.
Catatonia in Down syndrome; a treatable cause of regression.
Ghaziuddin N, Nassiri A, Miles JH. Ghaziuddin N, et al. Among authors: miles jh. Neuropsychiatr Dis Treat. 2015 Apr 2;11:941-9. doi: 10.2147/NDT.S77307. eCollection 2015. Neuropsychiatr Dis Treat. 2015. PMID: 25897230 Free PMC article.
51 results