Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Catherine Willoughby"'
Autor:
Paul Denny, Shoumo Bhattacharya, Andy Greenfield, Patrick M. Nolan, Jiannis Ragoussis, Gimara Duncan, Kulvinder Kaur, Andrea Hardy, Richard McKeone, Ramya Chandrasekara, Matthew Cadman, Steve D.M. Brown, Anju Paudyal, Jennifer R. Davies, Jürgen E. Schneider, Michael J. Depew, Paul T. Sharpe, Ruth M. Arkell, Nikos Tripodis, Ghazala Mirza, Debora Bogani, Heather Haines, Catherine Willoughby, Guido E Pieles
Publikováno v:
Proceedings of the National Academy of Sciences. 102:12477-12482
Monosomy of the human chromosome 6p terminal region results in a variety of congenital malformations that include brain, craniofacial, and organogenesis abnormalities. To examine the genetic basis of these phenotypes, we have carried out an unbiased
Autor:
Emma L. Baple, Deborah J G Mackay, Rebecca L. Poole, Catherine Willoughby, Rohan Taylor, Sahar Mansour, I. Karen Temple, Louise E Docherty
Publikováno v:
European journal of human genetics : EJHG. 19(3)
Angelman syndrome (AS) and Prader–Willi syndrome (PWS) are caused by genetic and epigenetic mutations of the imprinted gene cluster on chromosome 15q13. Although the imprinting mutations causing PWS and AS are essentially opposite in nature, remark
Autor:
Catherine Willoughby, Jo Ellen Crowe
Publikováno v:
Nursing Interventions for Infants, Children, and Families
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::152b9cbcf0000f0632f8c85c282dfe86
https://doi.org/10.4135/9781452220284.n27
https://doi.org/10.4135/9781452220284.n27
Autor:
Catherine Willoughby
Publikováno v:
Journal of Psychosocial Nursing and Mental Health Services. 33:6-6