OpenURL Connection Search

Select item for more details and to access through your institution.

Genetic studies on chromosome 12 in late-onset Alzheimer disease.
Published in:
1998
By:
- Wu, William S.;
- Holmans, Peter;
- Wavrant-DeVrieze, Fabienne;
- Shears, Shantia;
- Kehoe, Patrick;
- Crook, Richard;
- Booth, Jeremy;
- Williams, Nigel;
- Perez-Tur, Jordi;
- Roehl, Kimberely;
- Fenton, Iain;
- Chartier-Harlin, Marie-Christine;
- Lovestone, Simon;
- Williams, Julie;
- Hutton, Mike;
- Hardy, John;
- Owen, Michael J.;
- Goate, Alison;
- Wu, W S;
- Holmans, P
Publication type:
journal article
Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA<sub>3</sub>).
Published in:
Human Genetics, 2000, v. 106, n. 2, p. 206, doi. 10.1007/s004390051029
By:
- Rees, Mark I.;
- Watts, Patrick;
- Fenton, Iain;
- Clarke, Angus;
- Snell, Russell G.;
- Owen, Michael J.;
- Gray, Jonathan
Publication type:
Article
Human Gene Mutation Database-A biomedical information and research resource.
Published in:
Human Mutation, 2000, v. 15, n. 1, p. 45, doi. 10.1002/(SICI)1098-1004(200001)15:1<45::AID-HUMU10>3.0.CO;2-T
By:
- Krawczak, Michael;
- Ball, Edward V.;
- Fenton, Iain;
- Stenson, Peter D.;
- Abeysinghe, Shaun;
- Thomas, Nick;
- Cooper, David N.
Publication type:
Article
A full genome scan for late onset Alzheimer's disease.
Published in:
Human Molecular Genetics, 1999, v. 8, n. 2, p. 237, doi. 10.1093/hmg/8.2.237
By:
- Kehoe, Patrick;
- Wavrant-De Vrieze, Fabienne;
- Crook, Richard;
- Wu, William S.;
- Holmans, Peter;
- Fenton, Iain;
- Spurlock, Gillian;
- Norton, Nadine;
- Williams, Hywel;
- Williams, Nigel;
- Lovestone, Simon;
- Perez-Tur, Jordi;
- Hutton, Mike;
- Chartier-Harlin, Marie-Christine;
- Shears, Shantia;
- Roehl, Kimberly;
- Booth, Jeremy;
- Van Voorst, Wendy;
- Ramic, Dzanan;
- Williams, Julie
Publication type:
Article

Found: 4

Genetic studies on chromosome 12 in late-onset Alzheimer disease.

Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA<sub>3</sub>).

Human Gene Mutation Database-A biomedical information and research resource.

A full genome scan for late onset Alzheimer's disease.