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Journal of Medical Genetics|August 1, 1985
A population study of adult onset limb-girdle muscular dystrophyJ R Yates, A E EmeryTraffic (Copenhagen, Denmark)|February 24, 2001
Proteomic tools for cell biologyW H McDonald, J R YatesBritish Journal of Cancer|February 1, 1991
Familial renal cell carcinoma: clinical and molecular genetic aspectsE R Maher, J R YatesJournal of Cell Science|December 1, 1981
Cell-to-substrate contacts in an adhesion-defective mutant of Balb/c3T3 cellsJ R Yates, C S IzzardClinical Dysmorphology|April 20, 2001
A new case of Myhre syndromeM L Whiteford, W B Doig, P A Raine, et al.Journal of Medical Genetics|March 1, 1996
Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular studyE Reid, N Morrison, L Barron, et al.Clinical Dysmorphology|November 14, 1997
Spondylocostal dysostosis associated with a 46, XX,+15,dic(6;15)(q25;q11.2) translocationY J Crow, J L Tolmie, K Rippard, et al.Developmental Medicine and Child Neurology|April 1, 1996
X-linked hydrocephalus masquerading as spina bifida and destructive porencephaly in successive generations in one familyC M Brewer, B J Fredericks, J M Pont, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1996
Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven familiesM A Ahmed, E Reid, A Cooke, et al.Prenatal Diagnosis|February 1, 1987
Second trimester prenatal diagnosis of the Jarcho-Levin syndromeJ L Tolmie, M J Whittle, M B McNay, et al.Pageof 56