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Chromosome X marks the spot – TwinsUK

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Chromosome X marks the spot – TwinsUK
Using epigenomic studies in monozygotic twins to improve our understanding  of cancer

Using epigenomic studies in monozygotic twins to improve our understanding of cancer

India's Opportunities and Challenges in Establishing a Twin Registry: An  Unexplored Human Resource for the World's Second-Most Populous Nation, Twin Research and Human Genetics

India's Opportunities and Challenges in Establishing a Twin Registry: An Unexplored Human Resource for the World's Second-Most Populous Nation, Twin Research and Human Genetics

X Chromosome Contribution to the Genetic Architecture of Primary Biliary  Cholangitis - ScienceDirect

X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis - ScienceDirect

X Chromosome Contribution to the Genetic Architecture of Primary Biliary  Cholangitis - ScienceDirect

X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis - ScienceDirect

Novel genetic variants associated with lumbar disc degeneration in northern  Europeans: a meta-analysis of 4600 subjects

Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects

What colour are your eyes? Teaching the genetics of eye colour & colour  vision. Edridge Green Lecture RCOphth Annual Congress Glasgow May 2019

What colour are your eyes? Teaching the genetics of eye colour & colour vision. Edridge Green Lecture RCOphth Annual Congress Glasgow May 2019

Interferon inducible X-linked gene CXorf21 may contribute to sexual  dimorphism in Systemic Lupus Erythematosus

Interferon inducible X-linked gene CXorf21 may contribute to sexual dimorphism in Systemic Lupus Erythematosus

PDF) Quantitative Trait Loci for Bone Lengths on Chromosome 5 Using Dual  Energy X-Ray Absorptiometry Imaging in the Twins UK Cohort

PDF) Quantitative Trait Loci for Bone Lengths on Chromosome 5 Using Dual Energy X-Ray Absorptiometry Imaging in the Twins UK Cohort

Autosomal genetic variation is associated with DNA methylation in regions  variably escaping X-chromosome inactivation

Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation

Novel pleiotropic risk loci for melanoma and nevus density implicate  multiple biological pathways

Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

Genome-wide meta-analysis identifies genetic locus on chromosome 9  associated with Modic changes

Genome-wide meta-analysis identifies genetic locus on chromosome 9 associated with Modic changes

Escape from X-inactivation in twins exhibits intra- and inter-individual  variability across tissues and is heritable

Escape from X-inactivation in twins exhibits intra- and inter-individual variability across tissues and is heritable

Epigenomes, Free Full-Text

Epigenomes, Free Full-Text