4.7 Mb deletion encompassing TGFB2 associated with features of Loeys-Dietz syndrome and osteoporosis in adulthood.

Gaspar, Harald; Lutz, Bernd; Reicherter, Kerstin; Lühl, Simon; Taurman, Rita; Gabriel, Heinz; Brenner, Rolf E; Borck, Guntram (2017). 4.7 Mb deletion encompassing TGFB2 associated with features of Loeys-Dietz syndrome and osteoporosis in adulthood. American journal of medical genetics. Part A, 173(8), pp. 2289-2292. Wiley-Liss 10.1002/ajmg.a.38286

Full text not available from this repository.

Item Type:	Journal Article (Further Contribution)
Division/Institute:	04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Paediatric Medicine
UniBE Contributor:	Gaspar, Harald
Subjects:	600 Technology > 610 Medicine & health
ISSN:	1552-4825
Publisher:	Wiley-Liss
Language:	English
Submitter:	Anette van Dorland
Date Deposited:	16 Jan 2018 13:34
Last Modified:	05 Dec 2022 15:09
Publisher DOI:	10.1002/ajmg.a.38286
PubMed ID:	28544325
URI:	https://boris.unibe.ch/id/eprint/109122