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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1947 2
1959 1
1965 1
1990 1
1993 1
2005 3
2006 3
2008 1
2010 2
2011 1
2012 3
2013 3
2014 5
2015 3
2016 5
2017 5
2018 2
2019 4
2020 8
2021 7
2022 1
2023 6

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56 results

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Page 1
STAC3 Disorder.
Webb BD, Manoli I, Jabs EW. Webb BD, et al. 2019 Jun 20. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2019 Jun 20. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 31219695 Free Books & Documents. Review.
What Is Your Neurologic Diagnosis?
Schmidli FE, Webb BD, Guevar JJ. Schmidli FE, et al. Among authors: webb bd. J Am Vet Med Assoc. 2021 Mar 15;258(6):579-582. doi: 10.2460/javma.258.6.579. J Am Vet Med Assoc. 2021. PMID: 33683967 Free article. No abstract available.
Mitochondrial translation defects and human disease.
Webb BD, Diaz GA, Prasun P. Webb BD, et al. J Transl Genet Genom. 2020;4:71-80. doi: 10.20517/jtgg.2020.11. Epub 2020 May 23. J Transl Genet Genom. 2020. PMID: 33426504 Free PMC article.
Novel biallelic variants expand the phenotype of NAA20-related syndrome.
D'Onofrio G, Cuccurullo C, Larsen SK, Severino M, D'Amico A, Brønstad K, AlOwain M, Morrison JL, Wheeler PG, Webb BD, Alfalah A, Iacomino M, Uva P, Coppola A, Merla G, Salpietro VD, Zara F, Striano P, Accogli A, Arnesen T, Bilo L. D'Onofrio G, et al. Among authors: webb bd. Clin Genet. 2023 Sep;104(3):371-376. doi: 10.1111/cge.14359. Epub 2023 May 16. Clin Genet. 2023. PMID: 37191084
Genetic Advances in Craniofacial Malformations.
Webb BD, Taub PJ. Webb BD, et al. J Pediatr Genet. 2016 Dec;5(4):183. doi: 10.1055/s-0036-1592349. Epub 2016 Sep 14. J Pediatr Genet. 2016. PMID: 27895969 Free PMC article. No abstract available.
Inability to move one's face dampens facial expression perception.
Japee S, Jordan J, Licht J, Lokey S; Moebius Syndrome Research Consortium; Chen G, Snow J, Jabs EW, Webb BD, Engle EC, Manoli I, Baker C, Ungerleider LG. Japee S, et al. Among authors: webb bd. Cortex. 2023 Sep 30;169:35-49. doi: 10.1016/j.cortex.2023.08.014. Online ahead of print. Cortex. 2023. PMID: 37852041 Free article.
A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome.
Di Gioia SA, Connors S, Matsunami N, Cannavino J, Rose MF, Gilette NM, Artoni P, de Macena Sobreira NL, Chan WM, Webb BD, Robson CD, Cheng L, Van Ryzin C, Ramirez-Martinez A, Mohassel P, Leppert M, Scholand MB, Grunseich C, Ferreira CR, Hartman T, Hayes IM, Morgan T, Markie DM, Fagiolini M, Swift A, Chines PS, Speck-Martins CE, Collins FS, Jabs EW, Bönnemann CG, Olson EN; Moebius Syndrome Research Consortium; Carey JC, Robertson SP, Manoli I, Engle EC. Di Gioia SA, et al. Among authors: webb bd. Nat Commun. 2017 Jul 6;8:16077. doi: 10.1038/ncomms16077. Nat Commun. 2017. PMID: 28681861 Free PMC article.
56 results