Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Julian Barwell"'
Autor:
Eamonn R. Maher, Julian Adlard, Julian Barwell, Angela F. Brady, Paul Brennan, Jackie Cook, Gillian S. Crawford, Tabib Dabir, Rosemarie Davidson, Rebecca Dyer, Rachel Harrison, Claire Forde, Dorothy Halliday, Helen Hanson, Eleanor Hay, Jenny Higgs, Mari Jones, Fiona Lalloo, Zosia Miedzybrodzka, Kai Ren Ong, Frauke Pelz, Deborah Ruddy, Katie Snape, James Whitworth, Richard N. Sandford
Funder: NIHR Cambridge Biomedical Reserach Centre VHL Alliance UK
BACKGROUND: Von Hippel-Lindau (VHL) disease is an inherited tumour predisposition syndrome and a paradigm for the importance of early diagnosis and surveillance. However, there is
BACKGROUND: Von Hippel-Lindau (VHL) disease is an inherited tumour predisposition syndrome and a paradigm for the importance of early diagnosis and surveillance. However, there is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06295e83d0a66ef4ce1ca1c5157b288b
https://www.repository.cam.ac.uk/handle/1810/336508
https://www.repository.cam.ac.uk/handle/1810/336508
Autor:
Caron Billington, Matthew Perfirgines, Wendy Watson, Annette M. Cashmore, Julian Barwell, Nicola Suter-Giorgini, Joanne H. Singletary, Rory O'Sullivan, Elizabeth King, Emily Victoria Craft
Publikováno v:
Familial Cancer. 14:637-640
In 2011, the Leicestershire Clinical Genetics Department in collaboration with Macmillan Cancer Support initiated a project called Supporting Families with Cancer (SFWC). The project aimed to raise awareness of inherited cancers amongst both healthca
Autor:
Julian Barwell, Susan Bint, Pamela Warburton, Miranda Splitt, Caroline Mackie Ogilvie, Darryl J. Maxwell
Publikováno v:
European Journal of Human Genetics. 11:749-753
Neocentromeres are rare functional centromeres formed within noncentromeric chromosomal regions. We report the finding of a neocentromere in a very rare class II analphoid chromosome. This neocentromere was detected prenatally in a fetus with the kar
Autor:
Julian Barwell
Publikováno v:
Human Genetics. 123:433-433