Retinopathy induced in mice by targeted disruption of the rhodopsin gene von Humphries, Marian M., Rancourt, Derrick, Farrar, G. Jane, Kenna, Paul, Hazel, Mark, Bush, Ronald A., Sieving, Paul A., Sheils, Denise M., Creighton, Peter, Erven, Alexandra, Boros, Andras, Gulya, Karoly, Capecchi, Mario R., Humphries, Peter

Volltext

A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa von Farrar, G. Jane, Kenna, Paul, Jordan, Siobhán A., Kumar-Singh, Rajendra, Humphries, Marian M., Sharp, Elizabeth M., Sheils, Denise M., Humphries, Peter

Volltext

Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q von Jordan, Siobhán A., Farrar, G. Jane, Kenna, Paul, Humphries, Marian M., Sheils, Denise M., Kumar-Singh, Rajendra, Sharp, Elizabeth M., Soriano, Nuria, Ayuso, Carmen, Benitez, Javier, Humphries, Peter

Volltext

A mutation (met→arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex von Humphries, Marian M., Sheils, Denise M., Farrar, Gwyneth J., Kumar-Singh, Rajendra, Kenna, Paul F., Mansergh, Fiona C., Jordan, Siobhan A., Young, Marjory, Humphries, Peter

Volltext

Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of Ireland von Humphries, Marian M., Mansergh, Fiona C., Kiang, Anna-Sophie, Jordan, Siobhán A., Sheils, Denise M., Martin, Michael J., Farrar, G. Jane, Kenna, Paul F., Young, Marjorie M., Humphries, Peter

Volltext

Autosomal dominant retinitis pigmentosa: A novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree von Jane Farrar, G., Kenna, Paul, Jordan, Siobhán A., Kumar-Singh, Rajendra, Humphries, Marian M., Sharp, Elizabeth M., Sheils, Denise, Humphries, Peter

Volltext

Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3 von McWilliam, Peter, Farrar, G.Jane, Kenna, Paul, Bradley, Daniel G., Humphries, Marian M., Sharp, Elizabeth M., McConnell, David J., Lawler, Mark, Sheils, Denise, Ryan, Carmel, Stevens, Karen, Daiger, Stephen P., Humphries, P.

Volltext

Human Nidogen Gene: Identification of Multiple RFLP and Exclusion as Candidate Gene in a Family with Epidermolysis Bullosa (EBS2) with Evidence for Linkage to Chromosome 1 von Humphries, Marian, Nagayoshi, Toshiro, Sheils, Denise, Humphries, Peter, Uitto, Jouni

Volltext

SHEILA sings “Love” with choristers von Jean Paul Carrère(réalisateur)

Volltext bestellen