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Journal of Medical Genetics
|
February 1, 1995
Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele
R J Daniels, L Campbell, N R Rodrigues, et al.
Human Genetics
|
September 1, 1993
Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA)
K E Morrison, R J Daniels, G K Suthers, et al.
Genetic Epidemiology
|
February 17, 2001
Involvement of BRCA1 and BRCA2 in breast cancer in a western Finnish sub-population
K Pääkkönen, S Sauramo, L Sarantaus, et al.
Human Molecular Genetics
|
November 5, 1997
Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated population
T Laitinen, P Kauppi, J Ignatius, et al.
Clinical Genetics
|
August 8, 2009
Molecular analysis of the GNPTAB and GNPTG genes in 13 patients with mucolipidosis type II or type III - identification of eight novel mutations
M Encarnação, L Lacerda, R Costa, et al.
The Journal of Clinical Investigation
|
March 1, 1989
A role for apolipoprotein E, apolipoprotein A-I, and low density lipoprotein receptors in cholesterol transport during regeneration and remyelination of the rat sciatic nerve
J K Boyles, C D Zoellner, L J Anderson, et al.
Journal of Endocrinological Investigation
|
May 29, 2009
Mutation analysis of MEN1, HRPT2, CASR, CDKN1B, and AIP genes in primary hyperparathyroidism patients with features of genetic predisposition
O Vierimaa, A Villablanca, A Alimov, et al.
European Journal of Endocrinology
|
September 4, 2007
Multiple endocrine neoplasia type 1 in Northern Finland; clinical features and genotype phenotype correlation
O Vierimaa, T M L Ebeling, S Kytölä, et al.
Annals of Neurology
|
July 14, 2000
Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment
M M Guerreiro, E Andermann, R Guerrini, et al.
Journal of Medical Genetics
|
November 14, 1997
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study
A K Ryan, J A Goodship, D I Wilson, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 91) with videos related to
Sort By:
Page
of 10
Journal of Medical Genetics
|
February 1, 1995
Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele
R J Daniels, L Campbell, N R Rodrigues, et al.
Human Genetics
|
September 1, 1993
Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA)
K E Morrison, R J Daniels, G K Suthers, et al.
Genetic Epidemiology
|
February 17, 2001
Involvement of BRCA1 and BRCA2 in breast cancer in a western Finnish sub-population
K Pääkkönen, S Sauramo, L Sarantaus, et al.
Human Molecular Genetics
|
November 5, 1997
Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated population
T Laitinen, P Kauppi, J Ignatius, et al.
Clinical Genetics
|
August 8, 2009
Molecular analysis of the GNPTAB and GNPTG genes in 13 patients with mucolipidosis type II or type III - identification of eight novel mutations
M Encarnação, L Lacerda, R Costa, et al.
The Journal of Clinical Investigation
|
March 1, 1989
A role for apolipoprotein E, apolipoprotein A-I, and low density lipoprotein receptors in cholesterol transport during regeneration and remyelination of the rat sciatic nerve
J K Boyles, C D Zoellner, L J Anderson, et al.
Journal of Endocrinological Investigation
|
May 29, 2009
Mutation analysis of MEN1, HRPT2, CASR, CDKN1B, and AIP genes in primary hyperparathyroidism patients with features of genetic predisposition
O Vierimaa, A Villablanca, A Alimov, et al.
European Journal of Endocrinology
|
September 4, 2007
Multiple endocrine neoplasia type 1 in Northern Finland; clinical features and genotype phenotype correlation
O Vierimaa, T M L Ebeling, S Kytölä, et al.
Annals of Neurology
|
July 14, 2000
Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment
M M Guerreiro, E Andermann, R Guerrini, et al.
Journal of Medical Genetics
|
November 14, 1997
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study
A K Ryan, J A Goodship, D I Wilson, et al.
Page
of 10