Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly - Archive ouverte HAL Access content directly
Journal Articles Clinical Genetics Year : 2017

Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly

(1) , (1, 2) , (1) , (2) , (2) , (1) , (3) , (4) , (1) , (2, 1, 5) , (1)
1
2
3
4
5

Domains

Life Sciences [q-bio] Genetics Human genetics Life Sciences [q-bio]

Sandrine Couvet  : Connect in order to contact the contributor

https://www.hal.inserm.fr/inserm-03867929

Submitted on : Wednesday, November 23, 2022-3:37:02 PM

Last modification on : Saturday, November 26, 2022-8:31:19 AM

Not file

Dates and versions

inserm-03867929 , version 1 (23-11-2022)

Identifiers

Cite

A. Lavillaureix, S. Heide, S. Chantot-Bastaraud, I. Marey, B. Keren, et al.. Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly. Clinical Genetics, 2017, 92 (5), pp.556-558. ⟨10.1111/cge.13062⟩. ⟨inserm-03867929⟩

Export

BibTeX TEI Dublin Core DC Terms EndNote Datacite

Collections

INSERM UPMC CNRS ICM SORBONNE-UNIVERSITE SU-MEDECINE
0 View
0 Download

Altmetric

Share

Gmail Facebook Twitter LinkedIn More