The role of chromosome analysis in practice

Detection of diagnostically critical, often hidden, anomalies in complex karyotypes of haematological disorders using multicolour fluorescence in situ hybridization.

British journal of haematology·2001

Localized chromosomal mosaicism as a cause of dysmorphic development.

American journal of human genetics·1984

1-Deamino-8-D-arginine vasopressin and urine cyclic adenosine monophosphate excretion in diabetes insipidus.

Clinical pharmacology and therapeutics·1981

Combined oral L-dopa and propranolol for growth hormone provocation.

Southern medical journal·1979

Turner's syndrome: index case after 44 years (a tribute to Dr. Henry H. Turner).

The Journal of clinical endocrinology and metabolism·1978

Sleep patterns in growth hormone deficient children and age-matched controls: developmental considerations.

Neuroendocrinology·1977

Divergent prescribing paradigms in cardiovascular care: a comparative analysis of government and private healthcare settings in Goa, India.

Postgraduate medicine·2026

Ponatinib in CML and Ph+ ALL: balancing high efficacy with vascular safety.

Postgraduate medicine·2026

Managing patients with cardiovascular-kidney-metabolic syndrome: a guideline-driven practical guide for primary care physicians.

Postgraduate medicine·2026

CV risk: if you aren't testing ACR, you aren't seeing the full picture.

Postgraduate medicine·2026

Anti-TNF-induced vasculitis: analysis of data from the French national pharmacovigilance database.

Postgraduate medicine·2026

Relationship of serum nesfatin-1 levels with body mass index and c-reactive protein in patients presenting to the emergency department with epileptic seizures.

Postgraduate medicine·2026

Discovering reference-missing cell types in bulk transcriptomics.

Bioinformatics (Oxford, England)·2026

A homozygous lamin B receptor variant resulting in Pelger-Huët anomaly without skeletal dysplasia.

Nucleus (Austin, Tex.)·2026

ZATELLITE: a toolkit to visualize and manipulate human centromeres in live cells using synthetic zinc fingers.

bioRxiv : the preprint server for biology·2026

Recurrent Single-Nucleotide Insertions in the Mitochondrial Second Light-Strand Promoter Cause Tubulointerstitial Kidney Disease.

medRxiv : the preprint server for health sciences·2026

Structural determination of human nucleosomes reconstituted by the ExACT platform.

bioRxiv : the preprint server for biology·2026

The linker histone H1.4 condenses chromatin in maturing postmitotic neurons.

bioRxiv : the preprint server for biology·2026

Related Experiment Videos

The role of chromosome analysis in practice

Related Concept Videos

Detection of diagnostically critical, often hidden, anomalies in complex karyotypes of haematological disorders using multicolour fluorescence in situ hybridization.

Localized chromosomal mosaicism as a cause of dysmorphic development.

1-Deamino-8-D-arginine vasopressin and urine cyclic adenosine monophosphate excretion in diabetes insipidus.

Combined oral L-dopa and propranolol for growth hormone provocation.

Turner's syndrome: index case after 44 years (a tribute to Dr. Henry H. Turner).

Sleep patterns in growth hormone deficient children and age-matched controls: developmental considerations.

Divergent prescribing paradigms in cardiovascular care: a comparative analysis of government and private healthcare settings in Goa, India.

Ponatinib in CML and Ph+ ALL: balancing high efficacy with vascular safety.

Managing patients with cardiovascular-kidney-metabolic syndrome: a guideline-driven practical guide for primary care physicians.

CV risk: if you aren't testing ACR, you aren't seeing the full picture.

Anti-TNF-induced vasculitis: analysis of data from the French national pharmacovigilance database.

Relationship of serum nesfatin-1 levels with body mass index and c-reactive protein in patients presenting to the emergency department with epileptic seizures.

Discovering reference-missing cell types in bulk transcriptomics.

A homozygous lamin B receptor variant resulting in Pelger-Huët anomaly without skeletal dysplasia.

ZATELLITE: a toolkit to visualize and manipulate human centromeres in live cells using synthetic zinc fingers.

Recurrent Single-Nucleotide Insertions in the Mitochondrial Second Light-Strand Promoter Cause Tubulointerstitial Kidney Disease.

Structural determination of human nucleosomes reconstituted by the ExACT platform.

The linker histone H1.4 condenses chromatin in maturing postmitotic neurons.

Related Experiment Videos

The role of chromosome analysis in practice

Related Concept Videos

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