Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1994 3
1995 2
1996 5
1998 3
1999 4
2000 8
2001 2
2002 8
2003 6
2004 4
2005 4
2006 5
2007 5
2008 5
2009 6
2010 8
2011 6
2012 4
2013 7
2014 5
2015 5
2016 2
2017 2
2018 1
2019 4
2020 8
2021 1
2022 3
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

117 results

Results by year

Filters applied: . Clear all
Page 1
PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects.
Petit F, Longoni M, Wells J, Maser RS, Bogenschutz EL, Dysart MJ, Contreras HTM, Frénois F, Pober BR, Clark RD, Giampietro PF, Ropers HH, Hu H, Loscertales M, Wagner R, Ai X, Brand H, Jourdain AS, Delrue MA, Gilbert-Dussardier B, Devisme L, Keren B, McCulley DJ, Qiao L, Hernan R, Wynn J, Scott TM, Calame DG, Coban-Akdemir Z, Hernandez P, Hernandez-Garcia A, Yonath H, Lupski JR, Shen Y, Chung WK, Scott DA, Bult CJ, Donahoe PK, High FA. Petit F, et al. Among authors: devisme l. Am J Hum Genet. 2023 Oct 5;110(10):1787-1803. doi: 10.1016/j.ajhg.2023.09.002. Epub 2023 Sep 25. Am J Hum Genet. 2023. PMID: 37751738 Free PMC article.
Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotype.
Coste T, Aloui C, Petit F, Moutton S, Devisme L, Wells CF, Leboucq N, Verpillat P, Yvert M, Rivier F, Tournier-Lasserve E. Coste T, et al. Among authors: devisme l. Ultrasound Obstet Gynecol. 2022 Dec;60(6):805-811. doi: 10.1002/uog.26046. Ultrasound Obstet Gynecol. 2022. PMID: 35943828 Free PMC article.
[Cerebellar cortical dysplasia: MRI aspects and significance].
Soto Ares G, Deries B, Delmaire C, Devisme L, Ruchoux MM, Pruvo JP. Soto Ares G, et al. Among authors: devisme l. J Radiol. 2004 Jun;85(6 Pt 1):729-40. doi: 10.1016/s0221-0363(04)97675-5. J Radiol. 2004. PMID: 15243373 Review. French.
[Fetal thoracic MR imaging].
Robert Y, Cuilleret V, Vaast P, Devisme L, Mestdagh P, Boyer C, Storme L. Robert Y, et al. Among authors: devisme l. Arch Pediatr. 2003 Apr;10(4):340-6. doi: 10.1016/s0929-693x(03)00333-6. Arch Pediatr. 2003. PMID: 12818757 Review. French.
Radiographic features of osteogenesis imperfecta.
Renaud A, Aucourt J, Weill J, Bigot J, Dieux A, Devisme L, Moraux A, Boutry N. Renaud A, et al. Among authors: devisme l. Insights Imaging. 2013 Aug;4(4):417-29. doi: 10.1007/s13244-013-0258-4. Epub 2013 May 19. Insights Imaging. 2013. PMID: 23686748 Free PMC article.
[Practical questions in case of maternal death].
Van Cortenbosch B, Parmentier D, Roy JP, Devisme L, Houssaye C, Dumoulin M, Puech F, Subtil D. Van Cortenbosch B, et al. Among authors: devisme l. Gynecol Obstet Fertil. 2008 Oct;36(10):1012-21. doi: 10.1016/j.gyobfe.2008.05.008. Epub 2008 Sep 26. Gynecol Obstet Fertil. 2008. PMID: 18823811 Review. French.
Exome sequencing identifies the first genetic determinants of sirenomelia in humans.
Lecoquierre F, Brehin AC, Coutant S, Coursimault J, Bazin A, Finck W, Benoist G, Begorre M, Beneteau C, Cailliez D, Chenal P, De Jong M, Degré S, Devisme L, Francannet C, Gérard B, Jeanne C, Joubert M, Journel H, Laurichesse Delmas H, Layet V, Liquier A, Mangione R, Patrier S, Pelluard F, Petit F, Tillouche N, van Ravenswaaij-Arts C, Frebourg T, Saugier-Veber P, Gruchy N, Nicolas G, Gerard M. Lecoquierre F, et al. Among authors: devisme l. Hum Mutat. 2020 May;41(5):926-933. doi: 10.1002/humu.23998. Epub 2020 Mar 1. Hum Mutat. 2020. PMID: 32058622
117 results