Chromosome mutations: frequency at birth in humans

Male breast cancer, age and sex chromosome aneuploidy.

British journal of cancer·2013

Self-mixing flow sensor using a monolithic VCSEL array with parallel readout.

Optics express·2010

Molecular sieve properties of mesoporous silica with intraporous nanocarbon.

Chemical communications (Cambridge, England)·2010

Cancer risk in patients with constitutional chromosome deletions: a nationwide British cohort study.

British journal of cancer·2008

Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes.

Human mutation·2007

X chromosome loss and ageing.

Cytogenetic and genome research·2007

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Humangenetik·1975

Climate associated variations in the human serum albumin level.

Humangenetik·1975

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Humangenetik·1975

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Humangenetik·1975

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Humangenetik·1975

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Humangenetik·1975

Asymmetrical chromosomal utilization during zygotic genome activation.

Frontiers in bioinformatics·2026

DeepKaryo-Check: a two-stage automated screening framework for chromosomal numerical and structural abnormalities in clinical karyotype analysis.

Frontiers in cell and developmental biology·2026

Multiparametric analysis of sperm chromatin and ROS reveals the existence of subpopulations that are linked to embryo development after ICSI.

Scientific reports·2026

Repeat offenders: Satellite DNA sequence variation drives heterochromatin instability.

Science advances·2026

Nuclear Dynamics and Its Timing Regulation Revealed by Live-Cell Imaging.

Advances in experimental medicine and biology·2026

Oocyte Kinetochores at the Nexus of Meiotic Drive and Segregation Fidelity.

Advances in experimental medicine and biology·2026

Related Experiment Videos

Chromosome mutations: frequency at birth in humans

Related Concept Videos

Male breast cancer, age and sex chromosome aneuploidy.

Self-mixing flow sensor using a monolithic VCSEL array with parallel readout.

Molecular sieve properties of mesoporous silica with intraporous nanocarbon.

Cancer risk in patients with constitutional chromosome deletions: a nationwide British cohort study.

Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes.

X chromosome loss and ageing.

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Climate associated variations in the human serum albumin level.

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Asymmetrical chromosomal utilization during zygotic genome activation.

DeepKaryo-Check: a two-stage automated screening framework for chromosomal numerical and structural abnormalities in clinical karyotype analysis.

Multiparametric analysis of sperm chromatin and ROS reveals the existence of subpopulations that are linked to embryo development after ICSI.

Repeat offenders: Satellite DNA sequence variation drives heterochromatin instability.

Nuclear Dynamics and Its Timing Regulation Revealed by Live-Cell Imaging.

Oocyte Kinetochores at the Nexus of Meiotic Drive and Segregation Fidelity.

Related Experiment Videos

Chromosome mutations: frequency at birth in humans

Related Concept Videos

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