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

16 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Renal cell carcinoma and a constitutional t(11;22)(q23;q11.2): case report and review of the potential link between the constitutional t(11;22) and cancer.
Doyen J, Carpentier X, Haudebourg J, Hoch B, Karmous-Benailly H, Ambrosetti D, Fabas T, Amiel J, Lambert JC, Pedeutour F. Doyen J, et al. Among authors: karmous benailly h. Cancer Genet. 2012 Nov;205(11):603-7. doi: 10.1016/j.cancergen.2012.09.006. Epub 2012 Oct 30. Cancer Genet. 2012. PMID: 23117075
Delineation of a region responsible for panhypopituitarism in 20p11.2.
Dayem-Quere M, Giuliano F, Wagner-Mahler K, Massol C, Crouzet-Ozenda L, Lambert JC, Karmous-Benailly H. Dayem-Quere M, et al. Among authors: karmous benailly h. Am J Med Genet A. 2013 Jul;161A(7):1547-54. doi: 10.1002/ajmg.a.35921. Epub 2013 May 8. Am J Med Genet A. 2013. PMID: 23657910
Evolution of a patient with Bohring-Opitz syndrome.
Pierron S, Richelme C, Triolo V, Mas JC, Griffet J, Karmous-Benailly H, Quere M, Kaname T, Lambert JC, Giuliano F. Pierron S, et al. Am J Med Genet A. 2009 Aug;149A(8):1754-7. doi: 10.1002/ajmg.a.32910. Am J Med Genet A. 2009. PMID: 19606480
Is interstitial 8p23 microdeletion responsible of 46,XY gonadal dysgenesis? One case report from birth to puberty.
Wagner-Mahler K, Kurzenne JY, Gastaud F, Hoflack M, Panaia Ferrari P, Berard E, Giuliano F, Karmous-Benailly H, Moceri P, Jouannelle C, Bourcier M, Robart E, Morel Y. Wagner-Mahler K, et al. Among authors: karmous benailly h. Mol Genet Genomic Med. 2019 Mar;7(3):e558. doi: 10.1002/mgg3.558. Epub 2019 Jan 28. Mol Genet Genomic Med. 2019. PMID: 30690934 Free PMC article.
EPHA7 haploinsufficiency is associated with a neurodevelopmental disorder.
Lévy J, Schell B, Nasser H, Rachid M, Ruaud L, Couque N, Callier P, Faivre L, Marle N, Engwerda A, van Ravenswaaij-Arts CMA, Plutino M, Karmous-Benailly H, Benech C, Redon S, Boute O, Boudry Labis E, Rama M, Kuentz P, Assoumani J, Maldergem LV, Dupont C, Verloes A, Tabet AC. Lévy J, et al. Among authors: karmous benailly h. Clin Genet. 2021 Oct;100(4):396-404. doi: 10.1111/cge.14017. Epub 2021 Jul 1. Clin Genet. 2021. PMID: 34176129
Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis.
Grossmann V, Höckner M, Karmous-Benailly H, Liang D, Puttinger R, Quadrelli R, Röthlisberger B, Huber A, Wu L, Spreiz A, Fauth C, Erdel M, Zschocke J, Utermann G, Kotzot D. Grossmann V, et al. Clin Genet. 2010 Dec;78(6):548-53. doi: 10.1111/j.1399-0004.2010.01419.x. Clin Genet. 2010. PMID: 20584030
De novo 4q duplication/deletion in a fetus with a congenital heart defect.
Dayem-Quere M, Giuliano F, Massol C, Piche M, Paquis-Flucklinger V, Karmous-Benailly H. Dayem-Quere M, et al. Among authors: karmous benailly h. Am J Med Genet A. 2015 Aug;167A(8):1932-6. doi: 10.1002/ajmg.a.37005. Epub 2015 Jun 19. Am J Med Genet A. 2015. PMID: 26097191 No abstract available.
16 results