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Radiology|November 1, 1985
MR imaging of calcified intracranial lesionsB A Holland, W Kucharczyk, M Brant-Zawadzki, et al.Journal of Medical Genetics|February 1, 1990
Exclusion of COL2A1 as a candidate gene in a family with Wagner-Stickler syndromeA E Fryer, M Upadhyaya, M Littler, et al.Human Molecular Genetics|December 1, 1992
Analysis of mutations at the neurofibromatosis 1 (NF1) locusM Upadhyaya, M Shen, A Cherryson, et al.Journal of Medical Genetics|December 1, 1986
Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosomeN S Thomas, H Williams, L J Elsas, et al.Journal of Medical Genetics|October 1, 1991
A closely linked DNA marker for facioscapulohumeral disease on chromosome 4qM Upadhyaya, P W Lunt, M Sarfarazi, et al.American Journal of Human Genetics|July 1, 1988
X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosisJ Zonana, A Clarke, M Sarfarazi, et al.Clinical Genetics|September 11, 2002
Developing a quality scoring system for epidemiological surveys of genetic disordersL N Al-Jader, R G Newcombe, S Hayes, et al.Journal of Molecular Biology|April 1, 1994
Molecular structure at 1.8 A of mouse liver class pi glutathione S-transferase complexed with S-(p-nitrobenzyl)glutathione and other inhibitorsI García-Sáez, A Párraga, M F Phillips, et al.Cytogenetics and Cell Genetics|January 1, 1986
Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybridsJ D Brook, D J Shaw, N S Thomas, et al.Journal of Medical Genetics|June 1, 1985
Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosomeC S Brown, P L Pearson, N S Thomas, et al.Pageof 23