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Bone
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June 23, 2004
Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees
David A Good, Frances Busfield, Barbara H Fletcher, et al.
Plos One
|
October 17, 2012
Attention deficit hyperactivity disorder in Australian adults: prevalence, persistence, conduct problems and disadvantage
Jane L Ebejer, Sarah E Medland, Julius van der Werf, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 17, 2009
Exploring the association between severe respiratory syncytial virus infection and asthma: a registry-based twin study
Simon Francis Thomsen, Sophie van der Sluis, Lone G Stensballe, et al.
Behavior Genetics
|
May 19, 2009
Association study of common mitochondrial variants and cognitive ability
Enda M Byrne, Allan F McRae, David L Duffy, et al.
Human Molecular Genetics
|
July 10, 2007
Receptor function, dominant negative activity and phenotype correlations for MC1R variant alleles
Kimberley A Beaumont, Sri N Shekar, Sri L Shekar, et al.
Twin Research : the Official Journal of the International Society for Twin Studies
|
December 21, 2004
A deletion mutation in GDF9 in sisters with spontaneous DZ twins
Grant W Montgomery, Zhen Zhen Zhao, Anna J Marsh, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
December 21, 2005
Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin families
Belinda K Cornes, Sarah E Medland, Manuel A R Ferreira, et al.
Human Genetics
|
October 7, 2005
The EPAS1 gene influences the aerobic-anaerobic contribution in elite endurance athletes
Jennifer Henderson, Jason M Withford-Cave, David L Duffy, et al.
Melanoma Research
|
June 28, 2019
IRF4 rs12203592*T/T genotype is associated with nodular melanoma
Jenna E Rayner, Erin K McMeniman, David L Duffy, et al.
American Journal of Human Genetics
|
January 20, 2007
A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation
David L Duffy, Grant W Montgomery, Wei Chen, et al.
Page
of 15
Search research articles
Search
Showing results (61-70 of 147) with videos related to
Sort By:
Page
of 15
Bone
|
June 23, 2004
Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees
David A Good, Frances Busfield, Barbara H Fletcher, et al.
Plos One
|
October 17, 2012
Attention deficit hyperactivity disorder in Australian adults: prevalence, persistence, conduct problems and disadvantage
Jane L Ebejer, Sarah E Medland, Julius van der Werf, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 17, 2009
Exploring the association between severe respiratory syncytial virus infection and asthma: a registry-based twin study
Simon Francis Thomsen, Sophie van der Sluis, Lone G Stensballe, et al.
Behavior Genetics
|
May 19, 2009
Association study of common mitochondrial variants and cognitive ability
Enda M Byrne, Allan F McRae, David L Duffy, et al.
Human Molecular Genetics
|
July 10, 2007
Receptor function, dominant negative activity and phenotype correlations for MC1R variant alleles
Kimberley A Beaumont, Sri N Shekar, Sri L Shekar, et al.
Twin Research : the Official Journal of the International Society for Twin Studies
|
December 21, 2004
A deletion mutation in GDF9 in sisters with spontaneous DZ twins
Grant W Montgomery, Zhen Zhen Zhao, Anna J Marsh, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
December 21, 2005
Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin families
Belinda K Cornes, Sarah E Medland, Manuel A R Ferreira, et al.
Human Genetics
|
October 7, 2005
The EPAS1 gene influences the aerobic-anaerobic contribution in elite endurance athletes
Jennifer Henderson, Jason M Withford-Cave, David L Duffy, et al.
Melanoma Research
|
June 28, 2019
IRF4 rs12203592*T/T genotype is associated with nodular melanoma
Jenna E Rayner, Erin K McMeniman, David L Duffy, et al.
American Journal of Human Genetics
|
January 20, 2007
A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation
David L Duffy, Grant W Montgomery, Wei Chen, et al.
Page
of 15