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Journal of Lipid Research
|
August 1, 1982
Proposed nomenclature of apoE isoproteins, apoE genotypes, and phenotypes
V I Zannis, J L Breslow, G Utermann, et al.
American Journal of Human Genetics
|
March 26, 1999
mtDNA analysis of Nile River Valley populations: A genetic corridor or a barrier to migration?
M Krings, A E Salem, K Bauer, et al.
Clinical Genetics
|
June 30, 2010
Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis
V Grossmann, M Höckner, H Karmous-Benailly, et al.
Clinical Genetics
|
October 15, 2013
Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies
A Spreiz, E Haberlandt, M Baumann, et al.
European Journal of Human Genetics : EJHG
|
March 27, 1999
Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome
A Silahtaroglu, F A Hol, P K Jensen, et al.
American Journal of Human Genetics
|
March 21, 2000
Mutational spectrum in the Delta7-sterol reductase gene and genotype-phenotype correlation in 84 patients with Smith-Lemli-Opitz syndrome
M Witsch-Baumgartner, B U Fitzky, M Ogorelkova, et al.
European Journal of Human Genetics : EJHG
|
February 15, 2001
Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations
M Witsch-Baumgartner, E Ciara, J Löffler, et al.
Journal of Medical Genetics
|
October 30, 2007
Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations
M Witsch-Baumgartner, I Schwentner, M Gruber, et al.
Page
of 21
Search research articles
Search
Showing results (201-210 of 208) with videos related to
Sort By:
Page
of 21
You have reached the last page of results.
This site can display upto 208 results.
Journal of Lipid Research
|
August 1, 1982
Proposed nomenclature of apoE isoproteins, apoE genotypes, and phenotypes
V I Zannis, J L Breslow, G Utermann, et al.
American Journal of Human Genetics
|
March 26, 1999
mtDNA analysis of Nile River Valley populations: A genetic corridor or a barrier to migration?
M Krings, A E Salem, K Bauer, et al.
Clinical Genetics
|
June 30, 2010
Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis
V Grossmann, M Höckner, H Karmous-Benailly, et al.
Clinical Genetics
|
October 15, 2013
Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies
A Spreiz, E Haberlandt, M Baumann, et al.
European Journal of Human Genetics : EJHG
|
March 27, 1999
Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome
A Silahtaroglu, F A Hol, P K Jensen, et al.
American Journal of Human Genetics
|
March 21, 2000
Mutational spectrum in the Delta7-sterol reductase gene and genotype-phenotype correlation in 84 patients with Smith-Lemli-Opitz syndrome
M Witsch-Baumgartner, B U Fitzky, M Ogorelkova, et al.
European Journal of Human Genetics : EJHG
|
February 15, 2001
Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations
M Witsch-Baumgartner, E Ciara, J Löffler, et al.
Journal of Medical Genetics
|
October 30, 2007
Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations
M Witsch-Baumgartner, I Schwentner, M Gruber, et al.
Page
of 21