The 1985 human gene map and human gene mapping in 1985

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

Leukemia·2017

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia.

Leukemia·2016

MicroRNA-related sequence variations in human cancers.

Human genetics·2013

Recurrent and founder mutations in the PMS2 gene.

Clinical genetics·2012

Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

Clinical genetics·2011

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

Gut·2010

Gene mapping in marsupials and monotremes. II. Assignments to the X chromosome of dasyurid marsupials.

Cytogenetics and cell genetics·2012

Trisomy 17 in a bonobo (Pan paniscus) and deletion of 3q in a lowland gorilla (Gorilla gorilla gorilla): comparison with human trisomy 18 and human deletion 4q syndrome.

Cytogenetics and cell genetics·2002

A case of azoospermia in a bull carrying a Y-autosome reciprocal translocation.

Cytogenetics and cell genetics·2002

The pattern of phylogenomic evolution of the Canidae.

Cytogenetics and cell genetics·2002

Analysis of chromosomal aberrations involving chromosome 1q31-->q53 in a DMBA-induced rat fibrosarcoma cell line: amplification and overexpression of Jak2.

Cytogenetics and cell genetics·2002

The mouse Arhgef6 gene: cDNA sequence, expression analysis, and chromosome assignment.

Cytogenetics and cell genetics·2002

The causal role of plasma protein ratios in ulcerative colitis: insights from mendelian randomization and single-cell sequencing.

Open medicine (Warsaw, Poland)·2026

Molecular Characterization of TSC1 and TSC2 Variants in a Greek Cohort of Tuberous Sclerosis Complex Patients.

Human mutation·2026

Rare germline variants in canonical and candidate genes in apparently sporadic bilateral primary aldosteronism.

Journal of the Endocrine Society·2026

Specific whole-chromosome identification of the A01/C1 homoeologs through oligonucleotide-based chromosome painting in Brassica species.

The Plant journal : for cell and molecular biology·2026

A Novel Frameshift Variant in SPAG1 Likely Causes Primary Ciliary Dyskinesia in Cocker Spaniels in Australia.

Animal genetics·2026

Multi-omics identification of ZFPM2 and CD44 as key candidates for testicular size in sheep.

Theriogenology·2026

Related Experiment Videos

The 1985 human gene map and human gene mapping in 1985

Related Concept Videos

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia.

MicroRNA-related sequence variations in human cancers.

Recurrent and founder mutations in the PMS2 gene.

Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

Gene mapping in marsupials and monotremes. II. Assignments to the X chromosome of dasyurid marsupials.

Trisomy 17 in a bonobo (Pan paniscus) and deletion of 3q in a lowland gorilla (Gorilla gorilla gorilla): comparison with human trisomy 18 and human deletion 4q syndrome.

A case of azoospermia in a bull carrying a Y-autosome reciprocal translocation.

The pattern of phylogenomic evolution of the Canidae.

Analysis of chromosomal aberrations involving chromosome 1q31-->q53 in a DMBA-induced rat fibrosarcoma cell line: amplification and overexpression of Jak2.

The mouse Arhgef6 gene: cDNA sequence, expression analysis, and chromosome assignment.

The causal role of plasma protein ratios in ulcerative colitis: insights from mendelian randomization and single-cell sequencing.

Molecular Characterization of TSC1 and TSC2 Variants in a Greek Cohort of Tuberous Sclerosis Complex Patients.

Rare germline variants in canonical and candidate genes in apparently sporadic bilateral primary aldosteronism.

Specific whole-chromosome identification of the A01/C1 homoeologs through oligonucleotide-based chromosome painting in Brassica species.

A Novel Frameshift Variant in SPAG1 Likely Causes Primary Ciliary Dyskinesia in Cocker Spaniels in Australia.

Multi-omics identification of ZFPM2 and CD44 as key candidates for testicular size in sheep.

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The 1985 human gene map and human gene mapping in 1985

Related Concept Videos

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