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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

444 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.
Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Crétien A, Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rössler J, Le Merrer M, Yaniv I, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H. Dgany O, et al. Among authors: iolascon a. Am J Hum Genet. 2002 Dec;71(6):1467-74. doi: 10.1086/344781. Epub 2002 Nov 14. Am J Hum Genet. 2002. PMID: 12434312 Free PMC article.
Suppression of CDA II expression in a homozygote.
Beauchamp-Nicoud A, Schischmanoff PO, Alloisio N, Boivin P, Parsons SF, Mielot F, Tchernia G, Legrand A, Miraglia Del Giudice E, Gasparini P, Iolascon A, Wickramasinghe SN, Delaunay J. Beauchamp-Nicoud A, et al. Among authors: iolascon a. Br J Haematol. 1999 Sep;106(4):948-53. doi: 10.1046/j.1365-2141.1999.01626.x. Br J Haematol. 1999. PMID: 10519996 Free article.
The congenital dyserythropoietic anaemias.
Delaunay J, Iolascon A. Delaunay J, et al. Among authors: iolascon a. Baillieres Best Pract Res Clin Haematol. 1999 Dec;12(4):691-705. doi: 10.1053/beha.1999.0048. Baillieres Best Pract Res Clin Haematol. 1999. PMID: 10895259 Review.
A second locus mapping to 2q35-36 for familial pseudohyperkalaemia.
Carella M, d'Adamo AP, Grootenboer-Mignot S, Vantyghem MC, Esposito L, D'Eustacchio A, Ficarella R, Stewart GW, Gasparini P, Delaunay J, Iolascon A. Carella M, et al. Among authors: iolascon a. Eur J Hum Genet. 2004 Dec;12(12):1073-6. doi: 10.1038/sj.ejhg.5201280. Eur J Hum Genet. 2004. PMID: 15470366
444 results