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Chromosome-specific differences in the recombination landscape of spontaneous meiotic nondisjunction. [PDF]
Turcotte CA, Sekelsky J.
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Finishing a complete giraffe genome from telomere to telomere with Verkko-Fillet. [PDF]
Kim J +13 more
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Grand challenges in sex differences in immunology: problems the field must solve before biological sex can guide clinical practice. [PDF]
Flanagan KL, Kovats S.
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Chromosomal structural abnormalities and tissue-specific mosaicism: insights into false-negative noninvasive prenatal testing. [PDF]
Huang N +10 more
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Transforming Life Science Through Chromosome-Level Genome Assemblies. [PDF]
Kon T +7 more
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Escape from X-chromosome inactivation: from gene discovery to regulatory mechanisms. [PDF]
Simoncini C, Loda A.
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The spatial relationship of human chromosomes within the nuclei of normal and emerin-mutant cells
Mahy, N +5 more
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Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms, 2008
Fragile sites are heritable specific chromosome loci that exhibit an increased frequency of gaps, poor staining, constrictions or breaks when chromosomes are exposed to partial DNA replication inhibition. They constitute areas of chromatin that fail to compact during mitosis. They are classified as rare or common depending on their frequency within the
T, Lukusa, J P, Fryns
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Fragile sites are heritable specific chromosome loci that exhibit an increased frequency of gaps, poor staining, constrictions or breaks when chromosomes are exposed to partial DNA replication inhibition. They constitute areas of chromatin that fail to compact during mitosis. They are classified as rare or common depending on their frequency within the
T, Lukusa, J P, Fryns
openaire +2 more sources

