Cytogenetic characterization of an iris melanoma

SNP analysis of minimally evolved t(14;18)(q32;q21)-positive follicular lymphomas reveals a common copy-neutral loss of heterozygosity pattern.

Cytogenetic and genome research·2011

Chromosomal alterations in oligodendroglial tumours over multiple surgeries: is tumour progression associated with change in 1p/19q status?

Journal of neuro-oncology·2008

Distinctive patterns of BCL6 molecular alterations and their functional consequences in different subgroups of diffuse large B-cell lymphoma.

Leukemia·2007

A comprehensive genetic and histopathologic analysis identifies two subgroups of B-cell malignancies carrying a t(14;19)(q32;q13) or variant BCL3-translocation.

Leukemia·2007

Changes in optic nerve head blood flow in children with cerebral malaria and acute papilloedema.

Journal of neurology, neurosurgery, and psychiatry·2006

Leukocyte count as a predictor of death during remission induction in acute myeloid leukemia.

Leukemia & lymphoma·2006

A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia.

Cancer genetics and cytogenetics·2010

Translocation (3;8)(q27;q24) in two cases of triple hit lymphoma.

Cancer genetics and cytogenetics·2010

Screening for DNA copy number aberrations in mucinous adenocarcinoma arising from the minor salivary gland: two case reports.

Cancer genetics and cytogenetics·2010

Screening for common copy-number variants in cancer genes.

Cancer genetics and cytogenetics·2010

Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma.

Cancer genetics and cytogenetics·2010

Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization.

Cancer genetics and cytogenetics·2010

Narrow Band Imaging Improves Endoscopic Differentiation of Inverted Papillomas From Nasal Polyps.

The Laryngoscope·2026

Epidemiological, Clinical and Viral Genomic Features of Influenza Virus Infections Among Pilgrims During the Grand Magal of Touba Over 7 Years (2018-2024).

Journal of medical virology·2026

Delayed Diagnosis of Common Variable Immunodeficiency Revealed by Recurrent Respiratory Infections and Persistent Mediastinal Lymphadenopathy: A Case Report.

Cureus·2026

Association Between UGT1A9 rs13418420 Polymorphism and Propofol Induction Characteristics in Chinese Female Patients Undergoing Brief Gynecological Procedures.

Pharmacogenomics and personalized medicine·2026

Clinical pearls and pitfalls in inborn errors of immunity: An expert-derived framework for diagnostic pattern recognition.

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology·2026

Inebilizumab in AQP4-Seropositive NMOSD: One-Year Follow-Up From a Multicenter, Real-World Study.

Annals of clinical and translational neurology·2026

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Cytogenetic characterization of an iris melanoma

Related Concept Videos

SNP analysis of minimally evolved t(14;18)(q32;q21)-positive follicular lymphomas reveals a common copy-neutral loss of heterozygosity pattern.

Chromosomal alterations in oligodendroglial tumours over multiple surgeries: is tumour progression associated with change in 1p/19q status?

Distinctive patterns of BCL6 molecular alterations and their functional consequences in different subgroups of diffuse large B-cell lymphoma.

A comprehensive genetic and histopathologic analysis identifies two subgroups of B-cell malignancies carrying a t(14;19)(q32;q13) or variant BCL3-translocation.

Changes in optic nerve head blood flow in children with cerebral malaria and acute papilloedema.

Leukocyte count as a predictor of death during remission induction in acute myeloid leukemia.

A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia.

Translocation (3;8)(q27;q24) in two cases of triple hit lymphoma.

Screening for DNA copy number aberrations in mucinous adenocarcinoma arising from the minor salivary gland: two case reports.

Screening for common copy-number variants in cancer genes.

Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma.

Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization.

Narrow Band Imaging Improves Endoscopic Differentiation of Inverted Papillomas From Nasal Polyps.

Epidemiological, Clinical and Viral Genomic Features of Influenza Virus Infections Among Pilgrims During the Grand Magal of Touba Over 7 Years (2018-2024).

Delayed Diagnosis of Common Variable Immunodeficiency Revealed by Recurrent Respiratory Infections and Persistent Mediastinal Lymphadenopathy: A Case Report.

Association Between UGT1A9 rs13418420 Polymorphism and Propofol Induction Characteristics in Chinese Female Patients Undergoing Brief Gynecological Procedures.

Clinical pearls and pitfalls in inborn errors of immunity: An expert-derived framework for diagnostic pattern recognition.

Inebilizumab in AQP4-Seropositive NMOSD: One-Year Follow-Up From a Multicenter, Real-World Study.

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Cytogenetic characterization of an iris melanoma

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