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

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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:

André Schaller

Date Deposited:

16 Jan 2018 13:34

Last Modified:

16 Jan 2018 13:34

Publisher DOI:

10.1002/ajmg.a.38286

PubMed ID:

28544325

URI:

https://boris.unibe.ch/id/eprint/109122

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