Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
7 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
O'Donnell-Luria-Rodan syndrome: description of a second multinational cohort and refinement of the phenotypic spectrum.
J Med Genet. 2022 Jul;59(7):697-705. doi: 10.1136/jmedgenet-2020-107470. Epub 2021 Jul 28.
J Med Genet. 2022.
PMID: 34321323
Free PMC article.
Variants in DOCK3 cause developmental delay and hypotonia.
Wiltrout K, Ferrer A, van de Laar I, Namekata K, Harada T, Klee EW, Zimmerman MT, Cousin MA, Kempainen JL, Babovic-Vuksanovic D, van Slegtenhorst MA, Aarts-Tesselaar CD, Schnur RE, Andrews M, Shinawi M.
Wiltrout K, et al. Among authors: aarts tesselaar cd.
Eur J Hum Genet. 2019 Aug;27(8):1225-1234. doi: 10.1038/s41431-019-0397-2. Epub 2019 Apr 11.
Eur J Hum Genet. 2019.
PMID: 30976111
Free PMC article.
Item in Clipboard
De Novo ATP1A1 Variants in an Early-Onset Complex Neurodevelopmental Syndrome.
Dohrn MF, Rebelo AP, Srivastava S, Cappuccio G, Smigiel R, Malhotra A, Basel D, van de Laar I, Neuteboom RF, Aarts-Tesselaar C, Mahida S, Brunetti-Pierri N, Taft RJ, Züchner S.
Dohrn MF, et al. Among authors: aarts tesselaar c.
Neurology. 2022 Mar 15;98(11):440-445. doi: 10.1212/WNL.0000000000013276. Epub 2022 Feb 2.
Neurology. 2022.
PMID: 35110381
Free PMC article.
Item in Clipboard
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.
Cameron-Christie SR, Wells CF, Simon M, Wessels M, Tang CZN, Wei W, Takei R, Aarts-Tesselaar C, Sandaradura S, Sillence DO, Cordier MP, Veenstra-Knol HE, Cassina M, Ludwig K, Trevisson E, Bahlo M, Markie DM, Jenkins ZA, Robertson SP.
Cameron-Christie SR, et al. Among authors: aarts tesselaar c.
Am J Hum Genet. 2018 Jun 7;102(6):1115-1125. doi: 10.1016/j.ajhg.2018.04.008. Epub 2018 May 24.
Am J Hum Genet. 2018.
PMID: 29805041
Free PMC article.
Item in Clipboard
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.
Cameron-Christie SR, Wells CF, Simon M, Wessels M, Tang CZN, Wei W, Takei R, Aarts-Tesselaar C, Sandaradura S, Sillence DO, Cordier MP, Veenstra-Knol HE, Cassina M, Ludwig K, Trevisson E, Bahlo M, Markie DM, Jenkins ZA, Robertson SP.
Cameron-Christie SR, et al. Among authors: aarts tesselaar c.
Am J Hum Genet. 2019 Sep 5;105(3):669. doi: 10.1016/j.ajhg.2019.08.007.
Am J Hum Genet. 2019.
PMID: 31491409
Free PMC article.
No abstract available.
Item in Clipboard
[Health care transition in young people with intellectual disabilities: from generalist to generalist].
de Man SA, Aarts-Tesselaar CD, Festen DA.
de Man SA, et al. Among authors: aarts tesselaar cd.
Ned Tijdschr Geneeskd. 2014;158:A8072.
Ned Tijdschr Geneeskd. 2014.
PMID: 25406820
Dutch.
Item in Clipboard
Fatal neonatal parechovirus encephalitis.
van Zwol AL, Lequin M, Aarts-Tesselaar C, van der Eijk AA, Driessen GA, de Hoog M, Govaert P.
van Zwol AL, et al. Among authors: aarts tesselaar c.
BMJ Case Rep. 2009;2009:bcr05.2009.1883. doi: 10.1136/bcr.05.2009.1883. Epub 2009 Dec 14.
BMJ Case Rep. 2009.
PMID: 22171236
Free PMC article.
Item in Clipboard
Cite
Cite