Parental origin of de novo chromosome rearrangements

Acceptance of HIV-1 education & voluntary counselling/testing by & seroprevalence of HIV-1 among, pregnant women in rural south India.

The Indian journal of medical research·2007

Demonstration of Philadelphia chromosome negative abnormal clones in patients with chronic myelogenous leukemia during major cytogenetic responses induced by imatinib mesylate.

Leukemia·2003

SNRPN methylation patterns in germ cell tumors as a reflection of primordial germ cell development.

Genes, chromosomes & cancer·2001

Amphetamine, 3,4-methylenedioxymethamphetamine, lysergic acid diethylamide, and metabolites of the catecholamine neurotransmitters are agonists of a rat trace amine receptor.

Molecular pharmacology·2001

Interstitial duplication of the short arm of chromosome 1 in a newborn with congenital heart disease and multiple malformations.

American journal of medical genetics·2001

Chromosomes 1 and 12 abnormalities in pediatric germ cell tumors by interphase fluorescence in situ hybridization.

Cancer genetics and cytogenetics·2001

Optical genome mapping improves structural variant detection and characterization in syndromic and neurogenetic disorders.

Human genetics·2026

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

Human genetics·2026

Integrating genetic, historical, and demographic evidence to reconstruct Argentina's matrilineal ancestry.

Human genetics·2026

Expected costs and benefits of genetic counselling and germline genetic testing in metastatic prostate cancer.

Human genetics·2026

From targeted SCN1A analysis to whole exome sequencing: clinical utility and novel genetic findings in a Hungarian paediatric epilepsy cohort.

Human genetics·2026

Genomic characterization of historical Jinlingnan individuals: insights into genetic continuity and trans-Eurasian signals in eastern China.

Human genetics·2026

Sex without crossovers mimics clonal reproduction in Rhynchospora tenuis.

Nature·2026

Transcriptional activity generates chromatin motion that drives nuclear blebbing.

Molecular biology of the cell·2026

Protocol for identifying head direction cells in mice using in vivo extracellular recordings and juxtacellular labeling.

STAR protocols·2026

Parallel analysis of repeat expansions: an updated Clin-CATS workflow for nanopore R10 flow cells.

The Journal of molecular diagnostics : JMD·2026

Unravelling the structure-function features of Ani2, a dual chaperone from Schizosaccharomyces pombe.

International journal of biological macromolecules·2026

Sperm subpopulations differing in mitochondrial abundance show divergent nuclear allele frequencies.

PloS one·2026

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Parental origin of de novo chromosome rearrangements

Related Concept Videos

Acceptance of HIV-1 education & voluntary counselling/testing by & seroprevalence of HIV-1 among, pregnant women in rural south India.

Demonstration of Philadelphia chromosome negative abnormal clones in patients with chronic myelogenous leukemia during major cytogenetic responses induced by imatinib mesylate.

SNRPN methylation patterns in germ cell tumors as a reflection of primordial germ cell development.

Amphetamine, 3,4-methylenedioxymethamphetamine, lysergic acid diethylamide, and metabolites of the catecholamine neurotransmitters are agonists of a rat trace amine receptor.

Interstitial duplication of the short arm of chromosome 1 in a newborn with congenital heart disease and multiple malformations.

Chromosomes 1 and 12 abnormalities in pediatric germ cell tumors by interphase fluorescence in situ hybridization.

Optical genome mapping improves structural variant detection and characterization in syndromic and neurogenetic disorders.

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

Integrating genetic, historical, and demographic evidence to reconstruct Argentina's matrilineal ancestry.

Expected costs and benefits of genetic counselling and germline genetic testing in metastatic prostate cancer.

From targeted SCN1A analysis to whole exome sequencing: clinical utility and novel genetic findings in a Hungarian paediatric epilepsy cohort.

Genomic characterization of historical Jinlingnan individuals: insights into genetic continuity and trans-Eurasian signals in eastern China.

Sex without crossovers mimics clonal reproduction in Rhynchospora tenuis.

Transcriptional activity generates chromatin motion that drives nuclear blebbing.

Protocol for identifying head direction cells in mice using in vivo extracellular recordings and juxtacellular labeling.

Parallel analysis of repeat expansions: an updated Clin-CATS workflow for nanopore R10 flow cells.

Unravelling the structure-function features of Ani2, a dual chaperone from Schizosaccharomyces pombe.

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Parental origin of de novo chromosome rearrangements

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