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Genomics|July 1, 1989
The human alpha-amylase multigene family consists of haplotypes with variable numbers of genesP C Groot, M J Bleeker, J C Pronk, et al.Gene|May 30, 1988
Cloning and sequencing of rhesus monkey pepsinogen A cDNAM P Evers, B Zelle, J P Bebelman, et al.Genomics|September 1, 1990
Evolution of the human alpha-amylase multigene family through unequal, homologous, and inter- and intrachromosomal crossoversP C Groot, W H Mager, N V Henriquez, et al.Clinical Genetics|September 1, 1986
Pepsinogen A polymorphism in gastric mucosa and urine, with special reference to patients with gastric cancerB D Westerveld, G Pals, J Defize, et al.Nature Genetics|November 1, 1995
Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3J C Pronk, R A Gibson, A Savoia, et al.Journal of the Neurological Sciences|September 1, 1984
Linkage studies in autosomal dominant facioscapulohumeral muscular dystrophyG Padberg, A W Eriksson, W S Volkers, et al.Neurology|May 12, 2004
Arg113His mutation in eIF2Bepsilon as cause of leukoencephalopathy in adultsM S van der Knaap, P A J Leegwater, C G M van Berkel, et al.Cancer|March 1, 1987
Clinical significance of pepsinogen A isozymogens, serum pepsinogen A and C levels, and serum gastrin levelsB D Westerveld, G Pals, C B Lamers, et al.Neurology|January 28, 2004
Multiparametric MRI in a patient with adult-onset leukoencephalopathy with vanishing white matterA Gallo, M A Rocca, A Falini, et al.American Journal of Human Genetics|August 12, 1999
The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27P A Leegwater, A A Könst, B Kuyt, et al.Pageof 7