Lista de obras - Samarth Bhatt - Dominio Público Uruguay

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.

artículo científico publicado en 2012

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

artículo científico publicado en 2013

A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia

artículo científico publicado en 2011

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

scientific article published on 20 December 2016

A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5).

artículo científico publicado en 2012

A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

artículo científico publicado en 2009

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.

artículo científico publicado en 2013

Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder

artículo científico publicado en 2009

An unusual T-cell childhood acute lymphoblastic leukemia harboring a yet unreported near-tetraploid karyotype

artículo científico publicado en 2011

Aplastic anemia and Klinefelter syndrome

scientific article published on 01 October 2004

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

artículo científico publicado en 2015

BNDF methylation in mothers and newborns is associated with maternal exposure to war trauma.

artículo científico publicado en 2017

Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm

artículo científico publicado en 2007

Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11

artículo científico publicado en 2012

Children's Relationship With Their Pet Dogs and Genotype Predict Child-Pet Interaction in an Experimental Setting

scientific article published on 05 September 2018

Chromosome distribution in human sperm - a 3D multicolor banding-study

artículo científico publicado en 2008

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

artículo científico publicado en 2016

Complex translocation disrupting TCF4 and altering TCF4 isoform expression segregates as mild autosomal dominant intellectual disability

artículo científico publicado en 2016

Effect of Pet Dogs on Children's Perceived Stress and Cortisol Stress Response

artículo científico publicado en 2016

Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements

artículo científico publicado en 2011

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations

artículo científico publicado en 2009

Human Ring Chromosomes - New Insights for their Clinical Significance

artículo científico publicado en 2013

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

artículo científico publicado en 2012

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

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Microdeletion and microduplication syndromes

artículo científico publicado en 2012

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

artículo científico publicado en 2012

Molecular cytogenetics studies reveal unexpected chromosomal inversion as variant of t(12;21)(p13;q22) in child with B-cell precursor acute lymphoblastic leukemia

artículo científico publicado en 2011

Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon

artículo científico publicado en 2008

Prenatal Maternal Stress Predicts Methylation of Genes Regulating the Hypothalamic-Pituitary-Adrenocortical System in Mothers and Newborns in the Democratic Republic of Congo

artículo científico publicado en 2016

Putting a finger on the problem: Finger stick blood draw and immunization at the well-child exam elicit a cortisol response to stress among one-year-old children

artículo científico publicado en 2018

Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture

artículo científico publicado en 2009

Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats

artículo científico publicado en 2011

Lista de obras de Samarth Bhatt

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 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 karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid 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

A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5).

A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

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.

Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder

An unusual T-cell childhood acute lymphoblastic leukemia harboring a yet unreported near-tetraploid karyotype

Aplastic anemia and Klinefelter syndrome

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

BNDF methylation in mothers and newborns is associated with maternal exposure to war trauma.

Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm

Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11

Children's Relationship With Their Pet Dogs and Genotype Predict Child-Pet Interaction in an Experimental Setting

Chromosome distribution in human sperm - a 3D multicolor banding-study

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

Complex translocation disrupting TCF4 and altering TCF4 isoform expression segregates as mild autosomal dominant intellectual disability

Effect of Pet Dogs on Children's Perceived Stress and Cortisol Stress Response

Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations

Human Ring Chromosomes - New Insights for their Clinical Significance

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

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

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

Microdeletion and microduplication syndromes

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

Molecular cytogenetics studies reveal unexpected chromosomal inversion as variant of t(12;21)(p13;q22) in child with B-cell precursor acute lymphoblastic leukemia

Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon

Prenatal Maternal Stress Predicts Methylation of Genes Regulating the Hypothalamic-Pituitary-Adrenocortical System in Mothers and Newborns in the Democratic Republic of Congo

Putting a finger on the problem: Finger stick blood draw and immunization at the well-child exam elicit a cortisol response to stress among one-year-old children

Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture

Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats