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Developmental Medicine and Child Neurology|August 1, 1994
Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxiaS Bundey, C Hardy, S Vickers, et al.Journal of Medical Genetics|June 4, 1998
A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UKA C Hutchesson, S Bundey, M A Preece, et al.Seminars in Neonatology : SN|February 13, 2001
Congenital heart malformations: aetiology and associationsP Brennan, I D YoungJournal of Medical Genetics|October 4, 2002
Coffin-Lowry syndrome: clinical and molecular featuresA Hanauer, I D YoungJournal of Medical Genetics|November 1, 1987
Unknown syndrome: abnormal facies, congenital heart defects, hypothyroidism, and severe retardationI D Young, K SimpsonObstetrical & Gynecological Survey|April 1, 1987
Recurrence risks for common complications of pregnancy--a reviewL Mehta, I D YoungBritish Medical Journal (Clinical Research Ed.)|July 11, 1987
Lethal malformations and perinatal mortality: a 10 year review with comparison of ethnic differencesI D Young, M ClarkeThe British Journal of Ophthalmology|March 1, 1993
X linked exudative vitreoretinopathy: clinical features and genetic linkage analysisP Fullwood, J Jones, S Bundey, et al.Archives of Insect Biochemistry and Physiology|March 26, 2003
Eicosanoid involvement in the regulation of behavioral fever in the desert locust, Schistocerca gregariaS Bundey, S Raymond, P Dean, et al.The New England Journal of Medicine|February 24, 1994
Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinismS T Lee, R D Nicholls, S Bundey, et al.Pageof 18