Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders

pubmed: wnt1 2022-05-14

Summary:

CONCLUSION: The overlapping spectra of monogenic adult LBMD can be easily disentangled by genetic testing and the proposed clinical criteria can help to maximize the diagnostic yield.

Link:

https://pubmed.ncbi.nlm.nih.gov/35276006/?utm_source=Other&utm_medium=rss&utm_campaign=None&utm_content=16uwQpOeqFYN8R4TKOtwPy2utpqy9ex2oldalD2yF_fQHv2caq&fc=None&ff=20220514083854&v=2.17.6

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Exome » pubmed: wnt1

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Authors:

Ralf Oheim, Elena Tsourdi, Lothar Seefried, Gisela Beller, Max Schubach, Eik Vettorazzi, Julian Stürznickel, Tim Rolvien, Nadja Ehmke, Alena Delsmann, Franca Genest, Ulrike Krüger, Tomasz Zemojtel, Florian Barvencik, Thorsten Schinke, Franz Jakob, Lorenz C Hofbauer, Stefan Mundlos, Uwe Kornak

Date tagged:

05/14/2022, 08:38

Date published:

03/11/2022, 06:00