Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sophia Frentz"'
Autor:
Sophia Frentz
Publikováno v:
Queering Science Communication ISBN: 9781529224436
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a618bdfffe09843648207c322954d96d
https://doi.org/10.56687/9781529224436-007
https://doi.org/10.56687/9781529224436-007
Autor:
Stephen P. Robertson, Zandra A. Jenkins, Tracy Dudding, Margriet van Kogelenberg, Alison Macharg, George McGillivray, Stuart Sugito, Jacek Pilch, Raj P. Kapur, Nicola Foulds, Sophia Frentz, Mark C. Hannibal, Cheng Yee Chang, Sixto García-Miñaur, Scott Nightingale, David Markie, Richard J. Leventer, Timothy R. Morgan, Wenhua Wei
Publikováno v:
Human Mutation. 39:103-113
Loss-of-function mutations in the X-linked gene FLNA can lead to abnormal neuronal migration, vascular and cardiac defects, and congenital intestinal pseudo-obstruction (CIPO), the latter characterized by anomalous intestinal smooth muscle layering.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4bb3aadd28906fd00206706b1af6d87
https://doi.org/10.1002/humu.23355
https://doi.org/10.1002/humu.23355
Autor:
Sophia Frentz, Jenny Morton, Stephen P. Robertson, Andrew J. Sutherland-Smith, Timothy R. Morgan
Publikováno v:
American Journal of Medical Genetics Part A. 170:2706-2710
Recently, a newly identified autosomal recessive skeletal dysplasia was described characterized by calvarial abnormalities (including cranium bifidum, coronal, and lambdoid synostosis), oligodactyly, femoral bowing, narrow thorax, small pelvic bones,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04b89bd9fffe907558edfb4003de30b0
https://doi.org/10.1002/ajmg.a.37804
https://doi.org/10.1002/ajmg.a.37804
Autor:
Jenkins, Zandra A., Macharg, Alison, Chang, Cheng‐Yee, van Kogelenberg, Margriet, Morgan, Tim, Frentz, Sophia, Wei, Wenhua, Pilch, Jacek, Hannibal, Mark, Foulds, Nicola, McGillivray, George, Leventer, Richard J., García‐Miñaúr, Sixto, Sugito, Stuart, Nightingale, Scott, Markie, David M., Dudding, Tracy, Kapur, Raj P., Robertson, Stephen P.
Publikováno v:
Human Mutation; Jan2018, Vol. 39 Issue 1, p103-113, 11p
Autor:
Morton, Jenny E. V., Frentz, Sophia, Morgan, Tim, Sutherland‐Smith, Andrew J., Robertson, Stephen P.
Publikováno v:
American Journal of Medical Genetics. Part A; Oct2016, Vol. 170A Issue 10, p2706-2710, 5p
Autor:
Lindy A. Orthia, Tara Roberson
A book on queer themes and science communication is timely, if not well overdue. LGBTIQA+ people have unique contributions to make and issues to meet through science communication. So, bringing ‘queer'and ‘science communication'together is an imp
Autor:
Jo Chandler
From the furthest reaches of the universe to the microscopic world of our genes, science offers writers the kind of scope other subjects simply can't match. Good writing about science can be moving, funny, exhilarating or poetic, but it will always b