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Results by year

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

Year Number of Results
1993 3
2002 4
2003 5
2004 4
2005 8
2006 5
2007 3
2008 3
2009 6
2010 7
2011 4
2012 13
2013 5
2014 13
2015 4
2016 6
2017 1
2018 4
2019 4
2020 6
2021 4
2022 5
2023 3
2024 2

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Search Results

110 results

Results by year

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Page 1
STAC3 Disorder.
Webb BD, Manoli I, Jabs EW. Webb BD, et al. Among authors: jabs ew. 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; 1993–2024. 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; 1993–2024. PMID: 31219695 Free Books & Documents. Review.
ESCO2 Spectrum Disorder.
Vega H, Gordillo M, Jabs EW. Vega H, et al. Among authors: jabs ew. 2006 Apr 18 [updated 2020 Mar 26]. 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; 1993–2024. 2006 Apr 18 [updated 2020 Mar 26]. 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; 1993–2024. PMID: 20301332 Free Books & Documents. Review.
Treacher Collins Syndrome.
Katsanis SH, Jabs EW. Katsanis SH, et al. Among authors: jabs ew. 2004 Jul 20 [updated 2020 Aug 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; 1993–2024. 2004 Jul 20 [updated 2020 Aug 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; 1993–2024. PMID: 20301704 Free Books & Documents. Review.
Cleft Palate in Apert Syndrome.
Willie D, Holmes G, Jabs EW, Wu M. Willie D, et al. Among authors: jabs ew. J Dev Biol. 2022 Aug 11;10(3):33. doi: 10.3390/jdb10030033. J Dev Biol. 2022. PMID: 35997397 Free PMC article. Review.
Dear old dad.
Glaser RL, Jabs EW. Glaser RL, et al. Among authors: jabs ew. Sci Aging Knowledge Environ. 2004 Jan 21;2004(3):re1. doi: 10.1126/sageke.2004.3.re1. Sci Aging Knowledge Environ. 2004. PMID: 14736914 Review.
Choanal Atresia and Craniosynostosis: Development and Disease.
Lesciotto KM, Heuzé Y, Jabs EW, Bernstein JM, Richtsmeier JT. Lesciotto KM, et al. Among authors: jabs ew. Plast Reconstr Surg. 2018 Jan;141(1):156-168. doi: 10.1097/PRS.0000000000003928. Plast Reconstr Surg. 2018. PMID: 29280877 Free PMC article. Review.
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Tenney AP, Di Gioia SA, Webb BD, Chan WM, de Boer E, Garnai SJ, Barry BJ, Ray T, Kosicki M, Robson CD, Zhang Z, Collins TE, Gelber A, Pratt BM, Fujiwara Y, Varshney A, Lek M, Warburton PE, Van Ryzin C, Lehky TJ, Zalewski C, King KA, Brewer CC, Thurm A, Snow J, Facio FM, Narisu N, Bonnycastle LL, Swift A, Chines PS, Bell JL, Mohan S, Whitman MC, Staffieri SE, Elder JE, Demer JL, Torres A, Rachid E, Al-Haddad C, Boustany RM, Mackey DA, Brady AF, Fenollar-Cortés M, Fradin M, Kleefstra T, Padberg GW, Raskin S, Sato MT, Orkin SH, Parker SCJ, Hadlock TA, Vissers LELM, van Bokhoven H, Jabs EW, Collins FS, Pennacchio LA, Manoli I, Engle EC. Tenney AP, et al. Among authors: jabs ew. Nat Genet. 2023 Jul;55(7):1149-1163. doi: 10.1038/s41588-023-01424-9. Epub 2023 Jun 29. Nat Genet. 2023. PMID: 37386251 Free PMC article.
FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research.
Samuels BD, Aho R, Brinkley JF, Bugacov A, Feingold E, Fisher S, Gonzalez-Reiche AS, Hacia JG, Hallgrimsson B, Hansen K, Harris MP, Ho TV, Holmes G, Hooper JE, Jabs EW, Jones KL, Kesselman C, Klein OD, Leslie EJ, Li H, Liao EC, Long H, Lu N, Maas RL, Marazita ML, Mohammed J, Prescott S, Schuler R, Selleri L, Spritz RA, Swigut T, van Bakel H, Visel A, Welsh I, Williams C, Williams TJ, Wysocka J, Yuan Y, Chai Y. Samuels BD, et al. Among authors: jabs ew. Development. 2020 Sep 21;147(18):dev191213. doi: 10.1242/dev.191213. Development. 2020. PMID: 32958507 Free PMC article. Review.
Nonsyndromic craniosynostosis: novel coding variants.
Sewda A, White SR, Erazo M, Hao K, García-Fructuoso G, Fernández-Rodriguez I, Heuzé Y, Richtsmeier JT, Romitti PA, Reva B, Jabs EW, Peter I. Sewda A, et al. Among authors: jabs ew. Pediatr Res. 2019 Mar;85(4):463-468. doi: 10.1038/s41390-019-0274-2. Epub 2019 Jan 14. Pediatr Res. 2019. PMID: 30651579 Free PMC article.
110 results