Showing results (51-60 of 92) with videos related to
Sort By:
Pageof 10
Advances in Oto-Rhino-Laryngology|January 25, 2007
The genetics of otosclerosis: pedigree studies and linkage analysisS R Saeed, M Briggs, C Lobo, et al.The Journal of Laryngology and Otology|December 1, 1996
A clinical, genetic and audiological study of patients and families with unilateral vestibular schwannomas. II. Audiological findings in 93 patients with unilateral vestibular schwannomasW J Neary, V E Newton, S N Laoide-Kemp, et al.Journal of Medical Genetics|July 1, 1989
Testing for cystic fibrosis using allelic associationA J Ivinson, A P Read, R Harris, et al.Journal of Medical Genetics|January 1, 1988
Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosomeK E Davies, T J Smith, S Bundey, et al.Human Genetics|October 1, 1988
Patterns of exon deletions in Duchenne and Becker muscular dystrophyA P Read, R C Mountford, S M Forrest, et al.Transplantation|November 1, 1981
Matching for properdin factor B (Bf) in renal transplantationP A Dyer, P T Klouda, R W Johnson, et al.The Journal of Laryngology and Otology|July 1, 1996
A clinical, genetic and audiological study of patients and families with unilateral vestibular schwannomas. I. Clinical features of neurofibromatosis in patients with unilateral vestibular schwannomasW J Neary, V E Newton, S N Laoide-Kemp, et al.Journal of Medical Genetics|December 24, 1998
Differential diagnosis of type 2 neurofibromatosis: molecular discrimination of NF2 and sporadic vestibular schwannomasC L Wu, N Thakker, W Neary, et al.Human Molecular Genetics|November 1, 1995
The mutational spectrum in Waardenburg syndromeM Tassabehji, V E Newton, X Z Liu, et al.Human Molecular Genetics|June 13, 1998
An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxaM Tassabehji, K Metcalfe, J Hurst, et al.Pageof 10