Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus)

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).

Leukemia·2015

Monosomal karyotype in MDS: explaining the poor prognosis?

Leukemia·2013

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

Prognostic significance of serial determinations of lactate dehydrogenase (LDH) in the follow-up of patients with myelodysplastic syndromes.

Annals of oncology : official journal of the European Society for Medical Oncology·2008

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

Spatiotemporal development of sparse excitatory neuronal types within the deep mouse cortex.

iScience·2026

Extended genotype-phenotype spectrum of 17α-hydroxylase/17,20-lyase deficiency: a nine-case series featuring a novel mutation, suspected TART-like lesions, and multisystem involvement.

Frontiers in endocrinology·2026

Hippo signaling regulates dorsoventral patterning in Drosophila head and eye development.

iScience·2026

Liver androgen receptor knockout protects female mice from high fat diet-induced insulin resistance.

npj metabolic health and disease·2026

Sex chromosome dosage effects on human brain structure and function: a systematic review of neuroimaging findings in sex chromosome aneuploidies.

European journal of medical genetics·2026

Sociodemographic risk factors and WISC-IV cognitive profile in children with specific learning disorder: a case-control study.

Applied neuropsychology. Child·2026

Related Experiment Videos

Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus)

Related Concept Videos

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.

Prognostic significance of serial determinations of lactate dehydrogenase (LDH) in the follow-up of patients with myelodysplastic syndromes.

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.

Spatiotemporal development of sparse excitatory neuronal types within the deep mouse cortex.

Extended genotype-phenotype spectrum of 17α-hydroxylase/17,20-lyase deficiency: a nine-case series featuring a novel mutation, suspected TART-like lesions, and multisystem involvement.

Hippo signaling regulates dorsoventral patterning in Drosophila head and eye development.

Liver androgen receptor knockout protects female mice from high fat diet-induced insulin resistance.

Sex chromosome dosage effects on human brain structure and function: a systematic review of neuroimaging findings in sex chromosome aneuploidies.

Sociodemographic risk factors and WISC-IV cognitive profile in children with specific learning disorder: a case-control study.

Related Experiment Videos

Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus)

Related Concept Videos

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