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Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology.
Gold JA, Ruth C, Osann K, Flodman P, McManus B, Lee HS, Donkervoort S, Khare M, Roof E, Dykens E, Miller JL, Driscoll DJ, Butler MG, Heinemann J, Cassidy S, Kimonis VE. Gold JA, et al. Among authors: dykens e. Genet Med. 2014 Feb;16(2):164-9. doi: 10.1038/gim.2013.97. Epub 2013 Aug 8. Genet Med. 2014. PMID: 23928912 Free PMC article.
Behavioral phenotype of Smith-Magenis syndrome (del 17p11.2).
Smith AC, Dykens E, Greenberg F. Smith AC, et al. Among authors: dykens e. Am J Med Genet. 1998 Mar 28;81(2):179-85. doi: 10.1002/(sici)1096-8628(19980328)81:2<179::aid-ajmg10>;2-e. Am J Med Genet. 1998. PMID: 9613859 Review.
Prader-Willi and Angelman syndromes: sister imprinted disorders.
Cassidy SB, Dykens E, Williams CA. Cassidy SB, et al. Among authors: dykens e. Am J Med Genet. 2000 Summer;97(2):136-46. doi: 10.1002/1096-8628(200022)97:2<136::aid-ajmg5>;2-v. Am J Med Genet. 2000. PMID: 11180221 Review.
Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental Syndromes.
Veatch OJ, Malow BA, Lee HS, Knight A, Barrish JO, Neul JL, Lane JB, Skinner SA, Kaufmann WE, Miller JL, Driscoll DJ, Bird LM, Butler MG, Dykens EM, Gold JA, Kimonis V, Bacino CA, Tan WH, Kothare SV, Peters SU, Percy AK, Glaze DG. Veatch OJ, et al. Among authors: dykens em. Pediatr Neurol. 2021 Oct;123:30-37. doi: 10.1016/j.pediatrneurol.2021.07.009. Epub 2021 Jul 24. Pediatr Neurol. 2021. PMID: 34388423
138 results