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Interphase FISH screening for the LCR‐mediated common rearrangement of isochromosome 17q in primary myelofibrosis

American journal of hematology, 2005-08, Vol.79 (4), p.309-313

2005

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Molecular cytogenetic characterization of a familial der(1)del(1)(p36.33)dup(1)(p36.33p36.22) with variable phenotype

American journal of medical genetics. Part A, 2005-12, Vol.139A (2), p.136-140

2005

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Amplification of the RARA gene in acute myeloid leukemia: significant finding or coincidental observation?

Cancer genetics and cytogenetics, 2010-10, Vol.202 (1), p.33-37

2010

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Prenatal Diagnosis of a Fetus with Unbalanced Translocation (4;13)(p16;q32) with Overlapping Features of Patau and Wolf-Hirschhorn Syndromes

Fetal diagnosis and therapy, 2002-11, Vol.17 (6), p.347-351

2002

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Sonographic, pathologic and karyotypic findings in a rare case of placenta fenestrata

Fetal diagnosis and therapy, 2004-11, Vol.19 (6), p.479-482

2004

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

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

2004

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FISH for HER-2/neu in breast cancer: standardization makes the difference

Indian journal of cancer, 2004-10, Vol.41 (4), p.152-158

2004

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Concerning "14q(22) deletion in a familial case of anophthalmia with polydactyly"

American journal of medical genetics. Part A, 2004-04, Vol.126A (1), p.108-108

Velagaleti, Gopalrao V.N.

2004

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Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia

American journal of human genetics, 2005-04, Vol.76 (4), p.652

2005

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Cytogenetic findings in a case of nodular fasciitis of subclavicular region

Cancer genetics and cytogenetics, 2003-03, Vol.141 (2), p.160-163

2003

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Malignant peripheral nerve sheath tumor with rhabdomyoblastic differentiation (malignant triton tumor) with balanced t(7;9)(q11.2;p24) and unbalanced translocation der(16)t(1;16)(q23;q13)

Cancer genetics and cytogenetics, 2004-02, Vol.149 (1), p.23-27

2004

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Familial interstitial deletion of chromosome 4 (p15.2p16.1)

Annales de génétique, 2003-10, Vol.46 (4), p.453-458

2003

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A rapid and noninvasive method for detecting tissue-limited mosaicism: detection of i(12)(p10) in buccal smear from a child with Pallister-Killian syndrome

Genetic testing, 2003-09, Vol.7 (3), p.219-223

2003

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Expression of CD4 on peripheral blood granulocytes: a novel finding in a case of myelodysplastic syndrome in association with t(5;12)

Cancer genetics and cytogenetics, 2002-07, Vol.136 (1), p.38-42

2002

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Translocation (15;17) and trisomy 21 in the microgranular variant of acute promyelocytic leukemia

Cancer genetics and cytogenetics, 2002, Vol.132 (1), p.74-76

2002

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Interstitial deletion of 20q in a patient with Waldenström macroglobulinemia following chemotherapy

Cancer genetics and cytogenetics, 2002-01, Vol.132 (2), p.145-148

2002

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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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Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay

American journal of medical genetics, 2002-03, Vol.108 (3), p.198-204

2002

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Molecular cytogenetic characterization of a de novo unbalanced translocation leading to trisomy 17q25-->qter and monosomy 18p11.3-->pter in a girl with dysmorphic features

Clinical dysmorphology, 2003-01, Vol.12 (1), p.29-33

2003

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FISH for HER-2/neu in breast cancer: Standardization makes the difference

Indian journal of cancer, 2005-02, Vol.41 (4)

Gokhale Sumita, Gatalica Zoran, Mohammad Amin, Rampy AI, Velagaleti Gopalrao VN

2005

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DISCORDANT DIRECT AND CULTURE RESULTS FOLLOWING CHORIONIC VILLUS SAMPLING AND THE DIAGNOSIS OF A THIRD CELL LINE IN THE FETUS

Prenatal diagnosis, 1997-02, Vol.17 (2), p.170-172

1997

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Myelodysplasia and Mast Cell Leukemia with t(9;22)

Case reports in oncological medicine, 2017, Vol.2017, p.9249302-9249302

2017

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Trisomy 5p. A case report and review

Annales de génétique, 2000-07, Vol.43 (3), p.143-145

2000

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Acute myeloid leukemia associated with hemophagocytic syndrome and t(4;7)(q21;q36)

Cancer genetics and cytogenetics, 2000-10, Vol.122 (1), p.26-29

2000

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Patent ductus arteriosus and microdeletion 22q11 in a patient with Klinefelter syndrome

Annales de génétique, 2000-04, Vol.43 (2), p.105-107

2000

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Interphase FISH screening for the LCR‐mediated common rearrangement of isochromosome 17q in primary myelofibrosis

Molecular cytogenetic characterization of a familial der(1)del(1)(p36.33)dup(1)(p36.33p36.22) with variable phenotype

Amplification of the RARA gene in acute myeloid leukemia: significant finding or coincidental observation?

Prenatal Diagnosis of a Fetus with Unbalanced Translocation (4;13)(p16;q32) with Overlapping Features of Patau and Wolf-Hirschhorn Syndromes

Sonographic, pathologic and karyotypic findings in a rare case of placenta fenestrata

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

FISH for HER-2/neu in breast cancer: standardization makes the difference

Concerning "14q(22) deletion in a familial case of anophthalmia with polydactyly"

Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia

Cytogenetic findings in a case of nodular fasciitis of subclavicular region

Malignant peripheral nerve sheath tumor with rhabdomyoblastic differentiation (malignant triton tumor) with balanced t(7;9)(q11.2;p24) and unbalanced translocation der(16)t(1;16)(q23;q13)

Familial interstitial deletion of chromosome 4 (p15.2p16.1)

A rapid and noninvasive method for detecting tissue-limited mosaicism: detection of i(12)(p10) in buccal smear from a child with Pallister-Killian syndrome

Expression of CD4 on peripheral blood granulocytes: a novel finding in a case of myelodysplastic syndrome in association with t(5;12)

Translocation (15;17) and trisomy 21 in the microgranular variant of acute promyelocytic leukemia

Interstitial deletion of 20q in a patient with Waldenström macroglobulinemia following chemotherapy

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

Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay

Molecular cytogenetic characterization of a de novo unbalanced translocation leading to trisomy 17q25-->qter and monosomy 18p11.3-->pter in a girl with dysmorphic features

FISH for HER-2/neu in breast cancer: Standardization makes the difference

DISCORDANT DIRECT AND CULTURE RESULTS FOLLOWING CHORIONIC VILLUS SAMPLING AND THE DIAGNOSIS OF A THIRD CELL LINE IN THE FETUS

Myelodysplasia and Mast Cell Leukemia with t(9;22)

Trisomy 5p. A case report and review

Acute myeloid leukemia associated with hemophagocytic syndrome and t(4;7)(q21;q36)

Patent ductus arteriosus and microdeletion 22q11 in a patient with Klinefelter syndrome

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