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Human Molecular Genetics|June 22, 2000
Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashionN Blagitko, S Mergenthaler, U Schulz, et al.Human Molecular Genetics|August 1, 1993
No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissuesG Jansen, M Bartolomei, V Kalscheuer, et al.Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.Human Molecular Genetics|September 1, 1994
A Stickler syndrome gene is linked to chromosome 6 near the COL11A2 geneH G Brunner, S E van Beersum, M L Warman, et al.Human Genetics|August 1, 1992
Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutationH Traupe, D Müller, D Atherton, et al.Nature|March 24, 1983
Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosomeP Goodfellow, G Banting, D Sheer, et al.FEBS Letters|November 21, 1988
The human lactase-phlorizin hydrolase gene is located on chromosome 2T A Kruse, L Bolund, K H Grzeschik, et al.Journal of Medical Genetics|March 2, 1999
A new X linked neurodegenerative syndrome with mental retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric regionB C Hamel, P Wesseling, W O Renier, et al.Human Genetics|December 1, 1988
The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGKH G Brunner, A van Bennekom, E M Lambermon, et al.Human Genetics|March 1, 1993
X-linked myoclonus epilepsy explained as a maternally inherited mitochondrial disorderD D de Vries, I J de Wijs, G Wolff, et al.Pageof 21