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Hepatocyte differentiation of mesenchymal stem cells from human adipose tissue in vitro promotes hepatic integration in vivo

Gut, 2009-04, Vol.58 (4), p.570-581

2009

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Complex chromosomal rearrangements: origin and meiotic behavior

Human reproduction update, 2011-07, Vol.17 (4), p.476-494

2011

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Next generation phenotyping in Emanuel and Pallister‐Killian syndrome using computer‐aided facial dysmorphology analysis of 2D photos

Clinical genetics, 2018-02, Vol.93 (2), p.378-381

2018

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Small supernumerary marker chromosomes (sSMC) in humans

Cytogenetic and genome research, 2004-01, Vol.107 (1-2), p.55-67

2004

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Highly conserved Z and molecularly diverged W chromosomes in the fish genus Triportheus (Characiformes, Triportheidae)

Heredity, 2017-03, Vol.118 (3), p.276-283

2017

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Chromosomal breakpoints in a cohort of head and neck squamous cell carcinoma patients

Genomics (San Diego, Calif.), 2020-01, Vol.112 (1), p.297-303

2020

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Mouse white adipose tissue-derived mesenchymal stem cells gain pericentral and periportal hepatocyte features after differentiation in vitro, which are preserved in vivo after hepatic transplantation

Acta Physiologica, 2015-10, Vol.215 (2), p.89-104

2015

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7q11.23 microduplication syndrome: neurophysiological and neuroradiological insights into a rare chromosomal disorder

Journal of intellectual disability research, 2018-05, Vol.62 (5), p.359-370

2018

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Comparative Chromosomal Mapping of Microsatellites in Leporinus Species (Characiformes, Anostomidae): Unequal Accumulation on the W Chromosomes

Cytogenetic and genome research, 2014-01, Vol.142 (1), p.40-45

2014

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A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotype

Gene, 2014-02, Vol.536 (2), p.441-443

2014

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A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14)

Human genome variation, 2020-09, Vol.7 (1), p.28-28, Article 28

2020

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Independent Sex Chromosome Evolution in Lower Vertebrates: A Molecular Cytogenetic Overview in the Erythrinidae Fish Family

Cytogenetic and genome research, 2013-01, Vol.141 (2-3), p.186-194

2013

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Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21

Cancer genetics, 2022-04, Vol.262-263, p.16-22

2022

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Clinical Impact of Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes

Cytogenetic and genome research, 2013-01, Vol.139 (3), p.158-163

2013

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NTRK3 REARRANGEMENT IN A NON-ROBERTSONIAN T(15;21)(Q25.3;Q22.1) IN AN PEDIATRIC PATIENT WITH PROGENITOR B-CELL ACUTE LYMPHOBLASTIC LEUKEMIA WITH THE IAMP21

Hematology, Transfusion and Cell Therapy, 2021-10, Vol.43, p.S295-S296

2021

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QUANTITATIVE REAL-TIME PCR (RT-QPCR) COMPARING THE RELATIVE EXPRESSION LEVELS OF GENE TRANSCRIPTS INVOLVED IN A CRYPTIC THREE-WAY TRANSLOCATION T(9;11;19): AN ORIGINAL CASE OF AN INFANT WITH DISMAL PROGNOSIS ACUTE LYMPHOBLASTIC LEUKEMIA

Hematology, Transfusion and Cell Therapy, 2021-10, Vol.43, p.S300-S300

2021

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Comparative cytogenetic mapping of rRNA genes among naked catfishes: implications for genomic evolution in the Bagridae family

Genetics and molecular research, 2014-01, Vol.13 (4), p.9533-9542

2014

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Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation

Cytogenetic and genome research, 2006-01, Vol.112 (1-2), p.23-34

2006

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X-autosome and X-Y translocations in female carriers: X-chromosome inactivation easily detectable by 5-ethynyl-2-deoxyuridine (EdU)

Balkan journal of medical genetics, 2017-06, Vol.20 (1), p.87-90

2017

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Centromere-specific multicolour fluorescence in situ hybridization on human spermatocyte I and II metaphases

Human reproduction (Oxford), 2009-08, Vol.24 (8), p.2029-2033

2009

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First Case of a Neocentromere Formation in an Otherwise Normal Chromosome 7

Cytogenetic and genome research, 2010-06, Vol.128 (4), p.189-191

2010

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Inverted Segment Size and the Presence of Recombination Hot Spot Clusters Matter in Sperm Segregation Analysis

Cytogenetic and genome research, 2014-01, Vol.142 (2), p.145-149

2014

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Patterns of genomic imbalances in human solid tumors (Review)

International journal of oncology, 2000-02, Vol.16 (2), p.383

2000

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A Family with an Inverted Tandem Duplication 5q22.1q23.2

Cytogenetic and genome research, 2013-01, Vol.139 (1), p.65-70

2013

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Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay

Molecular cytogenetics, 2016-08, Vol.9 (1), p.55, Article 55

2016

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