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J Hallmayer

Showing results (61-70 of 68) with videos related to

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American Journal of Human Genetics|October 16, 1999
A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies)L Kalaydjieva, A Perez-Lezaun, D Angelicheva, et al.
Molecular Psychiatry|August 23, 2002
Association between presenilin-1 Glu318Gly mutation and familial Alzheimer's disease in the Australian populationK Taddei, C Fisher, S M Laws, et al.
Journal of Autism and Developmental Disorders|July 30, 1999
Exclusion of linkage to the HLA region in ninety multiplex sibships with autismT Rogers, L Kalaydjieva, J Hallmayer, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 26, 2001
Angiotensin-converting enzyme activity and the ACE Alu polymorphism in autosomal dominant polycystic kidney diseaseT Schiavello, V Burke, N Bogdanova, et al.
American Journal of Medical Genetics|September 22, 1999
Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autismB Salmon, J Hallmayer, T Rogers, et al.
Nature Genetics|October 1, 1996
Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24L Kalaydjieva, J Hallmayer, D Chandler, et al.
Nature Genetics|June 6, 2001
Association analysis of NOTCH4 loci in schizophrenia using family and population-based controlsP Sklar, S G Schwab, N M Williams, et al.
American Journal of Human Genetics|July 27, 1999
A genomic screen of autism: evidence for a multilocus etiologyN Risch, D Spiker, L Lotspeich, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
American Journal of Human Genetics|October 16, 1999
A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies)L Kalaydjieva, A Perez-Lezaun, D Angelicheva, et al.
Molecular Psychiatry|August 23, 2002
Association between presenilin-1 Glu318Gly mutation and familial Alzheimer's disease in the Australian populationK Taddei, C Fisher, S M Laws, et al.
Journal of Autism and Developmental Disorders|July 30, 1999
Exclusion of linkage to the HLA region in ninety multiplex sibships with autismT Rogers, L Kalaydjieva, J Hallmayer, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 26, 2001
Angiotensin-converting enzyme activity and the ACE Alu polymorphism in autosomal dominant polycystic kidney diseaseT Schiavello, V Burke, N Bogdanova, et al.
American Journal of Medical Genetics|September 22, 1999
Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autismB Salmon, J Hallmayer, T Rogers, et al.
Nature Genetics|October 1, 1996
Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24L Kalaydjieva, J Hallmayer, D Chandler, et al.
Nature Genetics|June 6, 2001
Association analysis of NOTCH4 loci in schizophrenia using family and population-based controlsP Sklar, S G Schwab, N M Williams, et al.
American Journal of Human Genetics|July 27, 1999
A genomic screen of autism: evidence for a multilocus etiologyN Risch, D Spiker, L Lotspeich, et al.
Pageof 7