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Myelodysplastic syndrome transforming to atypical chronic myeloid leukemia shows changes in its mutation allele frequency and acquisition of new mutations

Leukemia research reports, 2021-01, Vol.15, p.100248, Article 100248

2021

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Characterization of a breast cancer cell line derived from a germ-line BRCA1 mutation carrier

Cancer research (Chicago, Ill.), 1998-08, Vol.58 (15), p.3237-3242

1998

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Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1

American journal of human genetics, 1998-12, Vol.63 (6), p.1757-1766

1998

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Chromosomal localization of a human mucin gene (MUC8) and cloning of the cDNA corresponding to the carboxy terminus

American journal of respiratory cell and molecular biology, 1997-03, Vol.16 (3), p.232-241

1997

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De novo supernumerary ring chromosome 7: first report of a non-mosaic patient and review of the literature

Clinical genetics, 2002-03, Vol.61 (3), p.202-206

2002

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Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia

Journal of medical genetics, 2011-05, Vol.48 (5), p.299-307

2011

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Moving towards a syndrome: a review of 20 cases and a new case of non-mosaic tetrasomy 9p with long-term survival

Clinical genetics, 1997-07, Vol.52 (1), p.23-29

Tonk, Vijay S.

1997

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Coded-Cooperation based Multi-Relay Algorithm for Device-to-Device Communication in 5G Cellular Networks

Indian journal of science and technology, 2017-01, Vol.10 (4)

2017

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Characterization of paired tumor and non‐tumor cell lines established from patients with breast cancer

International journal of cancer, 1998-12, Vol.78 (6), p.766-774

1998

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Aberrant methylation of TMS1 in small cell, non small cell lung cancer and breast cancer

International journal of cancer, 2003-08, Vol.106 (2), p.198-204

2003

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Comparison between fluorescence in situ hybridization and classical cytogenetics in human tumors

Anticancer research, 1998-05, Vol.18 (3A), p.1351

1998

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Allelotyping demonstrates common and distinct patterns of chromosomal loss in human lung cancer types

Genes chromosomes & cancer, 1998-04, Vol.21 (4), p.308-319

1998

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Molecular cytogenetic characterization of a recombinant chromosome rec(22)dup(22q)inv(22)(p13q12.2)

American journal of medical genetics. Part A, 2004-01, Vol.124A (1), p.92-95

2004

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Two Distinct Forms of the 64,000 Mr Protein of the Cleavage Stimulation Factor Are Expressed in Mouse Male Germ Cells

Proceedings of the National Academy of Sciences - PNAS, 1999-06, Vol.96 (12), p.6763-6768

1999

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Trisomy 2, trisomy 20, and del(17p) as sole chromosomal abnormalities in three cases of hepatoblastoma

Genes chromosomes & cancer, 1994-11, Vol.11 (3), p.199-202

1994

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Aberrant methylation of the cyclin D2 promoter in primary small cell, nonsmall cell lung and breast cancers

International journal of cancer, 2003-11, Vol.107 (3), p.341-345

2003

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Ring chromosome 8 syndrome: Further characterization

American journal of medical genetics, 2000-01, Vol.90 (2), p.162-164

2000

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Rhabdoid tumor of the kidney with primitive neuroectodermal tumor of the central nervous system: Associated tumors with different histologic, cytogenetic, and molecular findings

Genes chromosomes & cancer, 1994-11, Vol.11 (3), p.146-152

1994

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Retinal pigment mosaicism in Pallister-Killian syndrome (mosaic tetrasomy 12p)

Archives of ophthalmology (1960), 1999-12, Vol.117 (12), p.1648

1999

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Case report: Denovo inherited 18p deletion in a mother-fetus pair with extremely variable expression, confirmed by fluorescence in situ hybridization (FISH) analysis

European journal of obstetrics & gynecology and reproductive biology, 1997-06, Vol.73 (2), p.193-196

1997

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Chronic Eosinophilic Leukemia and Hypereosinophilic Syndromes: Proposal for Classification, Literature Review, and Report of a Case with a Unique Chromosomal Abnormality

Cancer genetics and cytogenetics, 1998-12, Vol.107 (2), p.111-117

1998

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Disease associated balanced chromosome rearrangements (DBCR): report of two new cases

Annales de génétique, 2003, Vol.46 (1), p.37-43

2003

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Denovo inherited 18p deletion in a mother-fetus pair with extremely variable expression, confirmed by fluorescence in situ hybridization (FISH) analysis

European journal of obstetrics & gynecology and reproductive biology, 1997, Vol.73 (2), p.193-196

1997

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Myelodysplastic syndrome transforming to atypical chronic myeloid leukemia shows changes in its mutation allele frequency and acquisition of new mutations

Leukemia research reports, 2021, Vol.15, p.100248-100248

2021

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Autism spectrum disorder with microdeletion 10q26 by subtelomere FISH

Pediatric health, medicine and therapeutics, 2011-05, Vol.2 (default), p.49-53

2011

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Myelodysplastic syndrome transforming to atypical chronic myeloid leukemia shows changes in its mutation allele frequency and acquisition of new mutations

Characterization of a breast cancer cell line derived from a germ-line BRCA1 mutation carrier

Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1

Chromosomal localization of a human mucin gene (MUC8) and cloning of the cDNA corresponding to the carboxy terminus

De novo supernumerary ring chromosome 7: first report of a non-mosaic patient and review of the literature

Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia

Moving towards a syndrome: a review of 20 cases and a new case of non-mosaic tetrasomy 9p with long-term survival

Coded-Cooperation based Multi-Relay Algorithm for Device-to-Device Communication in 5G Cellular Networks

Characterization of paired tumor and non‐tumor cell lines established from patients with breast cancer

Aberrant methylation of TMS1 in small cell, non small cell lung cancer and breast cancer

Comparison between fluorescence in situ hybridization and classical cytogenetics in human tumors

Allelotyping demonstrates common and distinct patterns of chromosomal loss in human lung cancer types

Molecular cytogenetic characterization of a recombinant chromosome rec(22)dup(22q)inv(22)(p13q12.2)

Two Distinct Forms of the 64,000 Mr Protein of the Cleavage Stimulation Factor Are Expressed in Mouse Male Germ Cells

Trisomy 2, trisomy 20, and del(17p) as sole chromosomal abnormalities in three cases of hepatoblastoma

Aberrant methylation of the cyclin D2 promoter in primary small cell, nonsmall cell lung and breast cancers

Ring chromosome 8 syndrome: Further characterization

Rhabdoid tumor of the kidney with primitive neuroectodermal tumor of the central nervous system: Associated tumors with different histologic, cytogenetic, and molecular findings

Retinal pigment mosaicism in Pallister-Killian syndrome (mosaic tetrasomy 12p)

Case report: Denovo inherited 18p deletion in a mother-fetus pair with extremely variable expression, confirmed by fluorescence in situ hybridization (FISH) analysis

Chronic Eosinophilic Leukemia and Hypereosinophilic Syndromes: Proposal for Classification, Literature Review, and Report of a Case with a Unique Chromosomal Abnormality

Disease associated balanced chromosome rearrangements (DBCR): report of two new cases

Denovo inherited 18p deletion in a mother-fetus pair with extremely variable expression, confirmed by fluorescence in situ hybridization (FISH) analysis

Myelodysplastic syndrome transforming to atypical chronic myeloid leukemia shows changes in its mutation allele frequency and acquisition of new mutations

Autism spectrum disorder with microdeletion 10q26 by subtelomere FISH

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