Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Sandy, Raeburn"'
Autor:
Sandy Raeburn
Publikováno v:
Genetics and Insurance ISBN: 9781003423768
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e06bbbff34871a7cf3946933efe6bb5
https://doi.org/10.1201/9781003423768-9
https://doi.org/10.1201/9781003423768-9
Autor:
Nicholas JY Woodhouse, Omayma T Elshafie, Ali S Al-Mamari, Nagi HS Mohammed, Fatma Al-Riyami, Sandy Raeburn
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 10, Iss 1, Pp 80-83 (2010)
Objectives: We are seeing a progressive increase in the number of young patients with clinically defined maturity onset diabetes of the young (MODY) having a family history suggestive of a monogenic cause of their disease and no evidence of autoimmun
Externí odkaz:
https://doaj.org/article/6d27bbadd2414326b7aec767933806b6
Autor:
Sandy Raeburn
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 8, Iss 2, Pp 129-135 (2008)
NA
Externí odkaz:
https://doaj.org/article/c4ce641fe0ce4100b9e1ed3c9518c7b5
Autor:
Sandy Raeburn
Publikováno v:
Oman Journal of Ophthalmology, Vol 2, Iss 3, Pp 107-107 (2009)
Externí odkaz:
https://doaj.org/article/fe3252507fd446ce8936459ec0e00c80
Autor:
Mark Hirst, Samantha Knight, Kay Davies, Gareth Cross, Kevin Ocraft, Sandy Raeburn, Shauna Heeger, Deborah Eunpu, EdmundC Jenkins, Richard Lindenbaum, CarlS Dobkin, Xiao-Hua Ding, MichaelS Krawczun, W Ted Brown, Ponmani Goonewardena, Judy Willner, Cindy Benson, Dominique Heitz, Francois Rousseau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be1fe43cf49f992a6fb0b15ff7d0d884
https://ora.ox.ac.uk/objects/uuid:6cedf3b5-36f1-4893-8d20-04ec8f61aaa4
https://ora.ox.ac.uk/objects/uuid:6cedf3b5-36f1-4893-8d20-04ec8f61aaa4
Autor:
Coro Paisán-Ruiz, Volkmar Gieselmann, Matthias Eckhardt, Sandy Raeburn, Aisha Alkhayat Alshehhi, Katherine J. Dick, Naomi A. Sibtain, Michael A. Patton, Christos Proukakis, Wafa Bashir, Andrew H. Crosby, Henry Houlden, Roshan Koul, Helena Maier, Reza Sharifi
Publikováno v:
Human Mutation. 31:E1251-E1260
Hereditary spastic paraplegia (HSP) describes a heterogeneous group of inherited neurodegenerative disorders in which the cardinal pathological feature is upper motor neurone degeneration leading to progressive spasticity and weakness of the lower li
Publikováno v:
Leukemia & Lymphoma. 49:1407-1410
We report familial Hodgkin lymphoma (FHL) in three brothers of an Omani family with 13 children. Two brothers were diagnosed to have a nodular sclerosing Hodgkin lymphoma (NSHL), and a nodular lymp...
Autor:
Sandy Raeburn
Publikováno v:
Public Health Genomics. 5:102-109
This report summarises the controversy of genetic tests and insurance, with a focus on the UK situation during the past decade. UK experience provides insight for future strategies to help people with genetic disadvantages make insurance provision fo
Autor:
Sandy Raeburn
Publikováno v:
Human Fertility. 1:44-47
In the past few years, the major genetic causes of male infertility have been elucidated and many of these can now be treated using intracytoplasmic sperm injection (ICSI). This has raised a number of wider issues in the families of people with this
Publikováno v:
Journal of American Association for Pediatric Ophthalmology and Strabismus. 9:604-606
The syndrome of iris coloboma, ptosis, hypertelorism, and mental retardation (Online Mendelian Inheritance in Man -- OMIM # 243310), also known as the Baraitser-Winter syndrome, originally was described in a brother and sister and in an unrelated gir