Samarth S. Bhatt

Jena, TH 07743, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 15 publications

A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of TP53 in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia.

A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of TP53 in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia.

Journal: Molecular cytogenetics

Published: August 22, 2016

Chromosomes in a genome-wise order: evidence for metaphase architecture.

Chromosomes in a genome-wise order: evidence for metaphase architecture.

Journal: Molecular cytogenetics

Published: March 23, 2016

Insights into Sex Chromosome Evolution and Aging from the Genome of a Short-Lived Fish.

Insights into Sex Chromosome Evolution and Aging from the Genome of a Short-Lived Fish.

Journal: Cell

Published: June 03, 2015

Application of BAC-probes to visualize copy number variants (CNVs).

Application of BAC-probes to visualize copy number variants (CNVs).

Journal: Methods in molecular biology (Clifton, N.J.)

Published: September 21, 2014

Human Ring Chromosomes - New Insights for their Clinical Significance.

Human Ring Chromosomes - New Insights for their Clinical Significance.

Journal: Balkan journal of medical genetics : BJMG

Published: November 23, 2013

Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysis.

Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysis.

Journal: Cytogenetic and genome research

Published: August 12, 2013

A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion.

A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion.

Journal: Gene

Published: July 26, 2013

A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification.

A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification.

Journal: Cytogenetic and genome research

Published: March 18, 2013

Heteromorphic variants of chromosome 9.

Heteromorphic variants of chromosome 9.

Journal: Molecular cytogenetics

Published: January 29, 2013

A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone.

A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone.

Journal: Blood cells, molecules & diseases

Published: September 04, 2012

Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?

Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?

Journal: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology

Published: June 21, 2012

Molecular cytogenetic evaluation of the efficacy of photodynamic therapy by indocyanine green in breast adenocarcinoma MCF-7 cells.

Molecular cytogenetic evaluation of the efficacy of photodynamic therapy by indocyanine green in breast adenocarcinoma MCF-7 cells.

Journal: Photodiagnosis and photodynamic therapy

Published: April 04, 2012

Showing 1-12 of 15

Last Updated: 09/26/2026