Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomes

Revised recommendations from the CSO-HNS taskforce on performance of tracheotomy during the COVID-19 pandemic - what a difference a year makes.

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Validation of WHO classification-based Prognostic Scoring System (WPSS) for myelodysplastic syndromes and comparison with the revised International Prognostic Scoring System (IPSS-R). A study of the International Working Group for Prognosis in Myelodysplasia (IWG-PM).

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Monosomal karyotype in MDS: explaining the poor prognosis?

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Impact of adjunct cytogenetic abnormalities for prognostic stratification in patients with myelodysplastic syndrome and deletion 5q.

Leukemia·2010

Clinical outcome of pretreated B-cell chronic lymphocytic leukemia following alemtuzumab therapy: a retrospective study on various cytogenetic risk categories.

Annals of oncology : official journal of the European Society for Medical Oncology·2010

Gene expression signature of chronic lymphocytic leukaemia with Trisomy 12.

European journal of clinical investigation·2009

Loss-Of-Function CCM Gene Variants in Japanese Patients With Cerebral Cavernous Malformations.

Clinical genetics·2026

A New Case of Lethal Congenital Contracture Syndrome Type 3 With Hyperinsulinism and Optic Atrophy.

Clinical genetics·2026

Genetic Spectrum of Cholestasis in Tunisia and Diagnostic Yield of Next-Generation Sequencing: Case Series of 70 Patients.

Clinical genetics·2026

Childhood-Onset Filamin c Related Cardiomyopathy: Genotype-Phenotype Correlation and Outcome.

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A Homozygous Variant in DMRTB1 Is Associated With Non-Obstructive Azoospermia in Humans.

Clinical genetics·2026

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

Clinical genetics·2026

Patient and Clinical Characteristics Associated With Subsequent Suicide Attempt Among Youth in the Emergency Department With a Positive Suicide Risk Screen.

Annals of emergency medicine·2026

Absorbable Mesh Splenorrhaphy in an Adolescent with Blunt Splenic Rupture: A Case Report and Narrative Review.

African journal of paediatric surgery : AJPS·2026

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Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomes

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Revised recommendations from the CSO-HNS taskforce on performance of tracheotomy during the COVID-19 pandemic - what a difference a year makes.

Validation of WHO classification-based Prognostic Scoring System (WPSS) for myelodysplastic syndromes and comparison with the revised International Prognostic Scoring System (IPSS-R). A study of the International Working Group for Prognosis in Myelodysplasia (IWG-PM).

Monosomal karyotype in MDS: explaining the poor prognosis?

Impact of adjunct cytogenetic abnormalities for prognostic stratification in patients with myelodysplastic syndrome and deletion 5q.

Clinical outcome of pretreated B-cell chronic lymphocytic leukemia following alemtuzumab therapy: a retrospective study on various cytogenetic risk categories.

Gene expression signature of chronic lymphocytic leukaemia with Trisomy 12.

Loss-Of-Function CCM Gene Variants in Japanese Patients With Cerebral Cavernous Malformations.

A New Case of Lethal Congenital Contracture Syndrome Type 3 With Hyperinsulinism and Optic Atrophy.

Genetic Spectrum of Cholestasis in Tunisia and Diagnostic Yield of Next-Generation Sequencing: Case Series of 70 Patients.

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Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

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Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomes

Abstract:

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