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Molecular Psychiatry
|
May 30, 2012
A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental disease
C S Ku, C Polychronakos, E K Tan, et al.
Journal of the Neurological Sciences
|
October 25, 2016
Central nervous system involvement in multiple symmetric lipomatosis
V K Kimiskidis, V Papaliagkas, S Papagiannopoulos, et al.
Nature Genetics
|
March 1, 1997
Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus
P Vafiadis, S T Bennett, J A Todd, et al.
Diabetes & Metabolism
|
October 13, 2007
Minor contribution of SMAD7 and KLF10 variants to genetic susceptibility of type 2 diabetes
R Gutierrez-Aguilar, Y Benmezroua, B Balkau, et al.
Human Molecular Genetics
|
March 4, 2000
An imprinted locus associated with transient neonatal diabetes mellitus
R J Gardner, D J Mackay, A J Mungall, et al.
Journal of Pediatric Surgery
|
August 1, 1987
Management of thyroid nodules in children: a 20-year experience
J G Desjardins, A H Khan, P Montupet, et al.
Diabetologia
|
December 14, 2004
Neonatal diabetes, with hypoplastic pancreas, intestinal atresia and gall bladder hypoplasia: search for the aetiology of a new autosomal recessive syndrome
J Mitchell, Z Punthakee, B Lo, et al.
Journal of Medical Genetics
|
July 15, 2005
Type 1 diabetes and the OAS gene cluster: association with splicing polymorphism or haplotype?
M-C Tessier, H-Q Qu, R Fréchette, et al.
Genes and Immunity
|
December 4, 2009
rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype
A K Steck, E E Baschal, J M Jasinski, et al.
Nature Genetics
|
November 14, 1997
Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele. The IMDIAB Group
S T Bennett, A J Wilson, L Esposito, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 82) with videos related to
Sort By:
Page
of 9
Molecular Psychiatry
|
May 30, 2012
A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental disease
C S Ku, C Polychronakos, E K Tan, et al.
Journal of the Neurological Sciences
|
October 25, 2016
Central nervous system involvement in multiple symmetric lipomatosis
V K Kimiskidis, V Papaliagkas, S Papagiannopoulos, et al.
Nature Genetics
|
March 1, 1997
Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus
P Vafiadis, S T Bennett, J A Todd, et al.
Diabetes & Metabolism
|
October 13, 2007
Minor contribution of SMAD7 and KLF10 variants to genetic susceptibility of type 2 diabetes
R Gutierrez-Aguilar, Y Benmezroua, B Balkau, et al.
Human Molecular Genetics
|
March 4, 2000
An imprinted locus associated with transient neonatal diabetes mellitus
R J Gardner, D J Mackay, A J Mungall, et al.
Journal of Pediatric Surgery
|
August 1, 1987
Management of thyroid nodules in children: a 20-year experience
J G Desjardins, A H Khan, P Montupet, et al.
Diabetologia
|
December 14, 2004
Neonatal diabetes, with hypoplastic pancreas, intestinal atresia and gall bladder hypoplasia: search for the aetiology of a new autosomal recessive syndrome
J Mitchell, Z Punthakee, B Lo, et al.
Journal of Medical Genetics
|
July 15, 2005
Type 1 diabetes and the OAS gene cluster: association with splicing polymorphism or haplotype?
M-C Tessier, H-Q Qu, R Fréchette, et al.
Genes and Immunity
|
December 4, 2009
rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype
A K Steck, E E Baschal, J M Jasinski, et al.
Nature Genetics
|
November 14, 1997
Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele. The IMDIAB Group
S T Bennett, A J Wilson, L Esposito, et al.
Page
of 9