Chromosome constitution of gestational trophoblastic disease

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

Safety and lipoprotein(a)-lowering effects of Kylo-11, a non-canonical, long-duration small interfering RNA targeting lipoprotein(a): a first-in-human, randomised, double-blind, placebo-controlled, phase 1 trial.

Lancet (London, England)·2026

Generalised eruptive histiocytosis mimicking lymphoma relapse in a patient with previous diffuse large B-cell lymphoma.

Lancet (London, England)·2026

Physiotherapist-led care for musculoskeletal conditions in the emergency department (RESHAP-ED): a randomised controlled trial with economic evaluation.

Lancet (London, England)·2026

Systematic reviews and the needs of the adolescent transgender health care field.

Lancet (London, England)·2026

Pre-eclampsia.

Lancet (London, England)·2026

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Science (New York, N.Y.)·2026

Related Experiment Videos

Chromosome constitution of gestational trophoblastic disease

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.

Safety and lipoprotein(a)-lowering effects of Kylo-11, a non-canonical, long-duration small interfering RNA targeting lipoprotein(a): a first-in-human, randomised, double-blind, placebo-controlled, phase 1 trial.

Generalised eruptive histiocytosis mimicking lymphoma relapse in a patient with previous diffuse large B-cell lymphoma.

Physiotherapist-led care for musculoskeletal conditions in the emergency department (RESHAP-ED): a randomised controlled trial with economic evaluation.

Systematic reviews and the needs of the adolescent transgender health care field.

Pre-eclampsia.

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Related Experiment Videos

Chromosome constitution of gestational trophoblastic disease

Related Concept Videos

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