Trisomy of the long arm of human chromosome 1

Expression analysis and functional activity of interleukin-7 splice variants.

Genes and immunity·2008

Fanconi anemia: causes and consequences of genetic instability.

Genome dynamics·2008

Disruption of the FA/BRCA pathway in bladder cancer.

Cytogenetic and genome research·2007

Genetic instability syndromes with progeroid features.

Zeitschrift fur Gerontologie und Geriatrie·2007

A distinctive nuclear morphology in acute myeloid leukemia is strongly associated with loss of HLA-DR expression and FLT3 internal tandem duplication.

Leukemia·2004

Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction.

Cytogenetic and genome research·2003

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

Cell-cycle-resolved Hi-C reveals unexpected plasticity of A/B compartments across interphase.

eLife·2026

Identification and characterization of factors that govern apicoplast segregation in Toxoplasma gondii.

Nature communications·2026

A dedicated partitioning machinery ensures faithful inheritance of the apicoplast in Toxoplasma gondii.

Nature communications·2026

CLCN6 mutation in an Indian patient with rapidly progressive dementia.

Psychiatric genetics·2026

Neck vs Head Interspace Ratios in Hallux Valgus: A Reliability Analysis of First Metatarsal Radiographic Measurements.

The Journal of foot and ankle surgery : official publication of the American College of Foot and Ankle Surgeons·2026

S-Nitrosylation of glycogen phosphorylase regulates nuclear glycogenolysis and is impaired in metabolic liver disorders.

Science advances·2026

Related Experiment Videos

Trisomy of the long arm of human chromosome 1

Related Concept Videos

Expression analysis and functional activity of interleukin-7 splice variants.

Fanconi anemia: causes and consequences of genetic instability.

Disruption of the FA/BRCA pathway in bladder cancer.

Genetic instability syndromes with progeroid features.

A distinctive nuclear morphology in acute myeloid leukemia is strongly associated with loss of HLA-DR expression and FLT3 internal tandem duplication.

Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction.

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.

Cell-cycle-resolved Hi-C reveals unexpected plasticity of A/B compartments across interphase.

Identification and characterization of factors that govern apicoplast segregation in Toxoplasma gondii.

A dedicated partitioning machinery ensures faithful inheritance of the apicoplast in Toxoplasma gondii.

CLCN6 mutation in an Indian patient with rapidly progressive dementia.

Neck vs Head Interspace Ratios in Hallux Valgus: A Reliability Analysis of First Metatarsal Radiographic Measurements.

S-Nitrosylation of glycogen phosphorylase regulates nuclear glycogenolysis and is impaired in metabolic liver disorders.

Related Experiment Videos

Trisomy of the long arm of human chromosome 1

Related Concept Videos

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