The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43 von Hodgkinson, KA, Connors, SP, Merner, N, Haywood, A, Young, T-L, McKenna, WJ, Gallagher, B, Curtis, F, Bassett, AS, Parfrey, PS

Volltext

Premature death in adults with 22q11.2 deletion syndrome von Bassett, A S, Chow, E W C, Husted, J, Hodgkinson, K A, Oechslin, E, Harris, L, Silversides, C

Volltext

Location of a Major Susceptibility Locus for Familial Schizophrenia on Chromosome 1q21-q22 von Brzustowicz, Linda M., Hodgkinson, Kathleen A., Eva W. C. Chow, Honer, William G., Bassett, Anne S.

Volltext

Elevated rates of schizophrenia in a familial sample with mental illness and intellectual disability von Greenwood, C. M. T., Husted, J., Bomba, M. D., Hodgkinson, K. A., Bassett, A. S.

Volltext

Reproductive fitness in familial schizophrenia von Bassett, Anne S., Bury, Alison, Hodgkinson, Kathleen A., Honer, William G.

Volltext

Adult polycystic kidney disease: knowledge, experience, and attitudes to prenatal diagnosis von Hodgkinson, K A, Kerzin-Storrar, L, Watters, E A, Harris, R

Volltext

Diagnosis of adult polycystic kidney disease by genetic markers and ultrasonographic imaging in a voluntary family register von Elles, R G, Hodgkinson, K A, Mallick, N P, O'Donoghue, D J, Read, A P, Rimmer, S, Watters, E A, Harris, R

Volltext

Genetic Counselling for Schizophrenia in the Era of Molecular Genetics von Hodgkinson, Kathleen A, Murphy, Jillian, O'Neill, Sheri, Brzustowicz, Linda, Bassett, Anne S

Volltext

Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Is a Fully Penetrant, Lethal Arrhythmic Disorder Caused by a Missense Mutation in the TMEM43 Gene von Merner, Nancy D., Hodgkinson, Kathy A., Haywood, Annika F.M., Connors, Sean, French, Vanessa M., Drenckhahn, Jörg-Detlef, Kupprion, Christine, Ramadanova, Kalina, Thierfelder, Ludwig, McKenna, William, Gallagher, Barry, Morris-Larkin, Lynn, Bassett, Anne S., Parfrey, Patrick S., Young, Terry-Lynn

Volltext

Intrafamilial variability in cleidocranial dysplasia: A three generation family von Chitayat, David, Hodgkinson, Kathy A., Azouz, E. Michel

Volltext

Branchio-Oto-Renal syndrome: Further delineation of an underdiagnosed syndrome von Chitayat, David, Hodgkinson, Kathy A., Chen, Moy-Fong, Haber, George D., Nakishima, Shigeto, Sando, Isamu

Volltext

Recombination or heterogeneity: is there a second locus for adult polycystic kidney disease? von Elles, R G, Read, A P, Hodgkinson, K A, Watters, A, Harris, R

Volltext

Approaches to the Analysis of Production Activity at Archaeological Sites

Volltext bestellen

King syndrome: A genetically heterogenous phenotype due to congenital myopathies von Chitayat, David, Hodgkinson, Kathy A., Ginsburg, Ophira, Dimmick, James, Watters, Gordon V.

Volltext

Robin sequence with facial and digital anomalies in two half-brothers by the same mother von CHITAYAT, D, MEUNIER, C. M, HODGKINSON, K. A, AZOUZ, M. E

Volltext

Mucolipidosis type IV: Clinical manifestations and natural history von Chitayat, David, Meunier, Catherine M., Hodgkinson, Kathy A., Silver, Kenneth, Flanders, Michael, Anderson, Ilse J., Little, John M., Whiteman, David A. H., Carpenter, Stirling

Volltext

The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5) von Hodgkinson, Kathy A., Parfrey, Patrick S., Bassett, Anne S., Kupprion, Christine, Drenckhahn, Jörg, Norman, Mark W., Thierfelder, Ludwig, Stuckless, Susan N., Dicks, Elizabeth L., McKenna, William J., Connors, Sean P.

Volltext

Linkage Disequilibrium Mapping of Schizophrenia Susceptibility to the CAPON Region of Chromosome 1q22 von Brzustowicz, Linda M., Simone, Jaime, Mohseni, Paria, Hayter, Jared E., Hodgkinson, Kathleen A., Chow, Eva W.C., Bassett, Anne S.

Volltext

Syndrome of mental retardation and distal arthrogryposis in sibs von Chitayat, David, Hodgkinson, Kathy A., Blaichman, Shirley, Chen, Moy-Fong, Watters, Gordon V., Khalife, Samir, Hall, Judith G.

Volltext

Acrania: A manifestation of the Adams-Oliver syndrome von Chitayat, David, Meunier, Catherine, Hodgkinson, Kathy A., Robb, Laura, Azouz, Michael

Volltext