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Double aneuploidy of trisomy 18 and Klinefelter syndrome: prenatal diagnosis and perinatal outcome

Journal of perinatal medicine, 2010, Vol.38 (5), p.565-566

2010

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Double aneuploidy of trisomy 18 and Klinefelter syndrome: prenatal diagnosis and perinatal outcome

Journal of perinatal medicine, 2010-09, Vol.38 (5), p.565-566

2010

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Correlation between ultrasonic velocity and indentation-based mechanical properties with microstructure in Nimonic 263

Materials science & engineering. A, Structural materials : properties, microstructure and processing, 2008-08, Vol.488 (1), p.398-405

2008

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Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) de novo in a child with dysmorphic features and streaky pigmentation: case report

Molecular cytogenetics, 2008-08, Vol.1 (1), p.19-19

2008

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Incidence of Down syndrome in Dubai, UAE

Medical principles and practice, 2007-01, Vol.16 (1), p.25-28

2007

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A complex translocation (6;12;8)(q25;q24.3;q13) in a fibrous hamartoma of infancy

Cancer genetics and cytogenetics, 2006-12, Vol.171 (2), p.115-118

2006

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Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: Clinical and genetic analysis

American journal of medical genetics. Part A, 2006-07, Vol.140A (13), p.1440-1446

2006

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Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred arab family with an apparent autosomal dominant inheritance and reduced penetrance : Clinical and genetic analysis: Split hand foot malformation

American journal of medical genetics. Part A, 2006, Vol.140 (13), p.1440-1446

2006

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New approaches to fluorescence in situ hybridization

Methods in molecular biology (Clifton, N.J.), 2006, Vol.319, p.237

2006

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Copy Number Analysis of c- erb -B2 ( HER-2/neu ) and Topoisomerase IIα Genes in Breast Carcinoma by Quantitative Real-Time Polymerase Chain Reaction Using Hybridization Probes and Fluorescence In Situ Hybridization

Archives of pathology & laboratory medicine (1976), 2005-01, Vol.129 (1), p.39-46

2005

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Copy Number Analysis of c-erb-B2 (HER-2/neu) and Topoisomerase II[alpha] Genes in Breast Carcinoma by Quantitative Real-Time Polymerase Chain Reaction Using Hybridization Probes and Fluorescence In Situ Hybridization

Archives of pathology & laboratory medicine (1976), 2005-01, Vol.129 (1), p.39

2005

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Copy number analysis of c-erb-B2 (HER-2/neu) and topoisomerase IIalpha genes in breast carcinoma by quantitative real-time polymerase chain reaction using hybridization probes and fluorescence in situ hybridization

Archives of pathology & laboratory medicine (1976), 2005-01, Vol.129 (1), p.39

2005

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Loss of Heterozygosity Associated with Uniparental Disomy in Breast Carcinoma

Modern pathology, 2002-12, Vol.15 (12), p.1241-1250

2002

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Gene encoding protein elongation factor EEF1A2 is a putative oncogene in ovarian cancer

Nature genetics, 2002-07, Vol.31 (3), p.301-305

2002

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Protein elongation factor EEF1A2 is a putative oncogene in ovarian cancer

Nature genetics, 2002-07, Vol.31 (3), p.301-305

2002

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[6] Fluorescence in Situ hybridization of LCM-isolated nuclei from paraffin sections

Methods in Enzymology, 2002, Vol.356, p.63-69

2002

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The retinal rod and cone Na+/Ca2+-K+ exchangers

Advances in experimental medicine and biology, 2002, Vol.514, p.237

2002

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Laser Capture Microdissection–Guided Fluorescence In Situ Hybridization and Flow Cytometric Cell Cycle Analysis of Purified Nuclei from Paraffin Sections

Modern pathology, 2000-06, Vol.13 (6), p.705-711

2000

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Hyperthermic induction of premature chromosome condensation in human lymphocytes

Mutation research, 1995-10, Vol.331 (2), p.175-180

1995

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Cytogenetic studies in a population suspected to have chromosomal abnormalities

Indian journal of pediatrics, 1990-03, Vol.57 (2), p.235-243

1990

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Down syndrome in Ahmedabad: karyotype analysis in 60 cases

Indian journal of pediatrics, 1987-09, Vol.54 (5), p.723-727

1987

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Trisomy 21 q: 46,XX,21s+/47,XX,+21q−(q22→qter) mosaicism (de novo) in a down syndrome child

Indian journal of pediatrics, 1984-05, Vol.51 (3), p.363-366

1984

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True hermaphrodite: 46, ;XX/46, XY, clinical, cytogenetic and histopathological studies

Indian journal of pediatrics, 1982-11, Vol.49 (6), p.885-890

1982

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Under-representation of older Indian persons with cancer in clinical trials

Double aneuploidy of trisomy 18 and Klinefelter syndrome: prenatal diagnosis and perinatal outcome

Double aneuploidy of trisomy 18 and Klinefelter syndrome: prenatal diagnosis and perinatal outcome

Correlation between ultrasonic velocity and indentation-based mechanical properties with microstructure in Nimonic 263

Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) de novo in a child with dysmorphic features and streaky pigmentation: case report

Incidence of Down syndrome in Dubai, UAE

A complex translocation (6;12;8)(q25;q24.3;q13) in a fibrous hamartoma of infancy

Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: Clinical and genetic analysis

Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred arab family with an apparent autosomal dominant inheritance and reduced penetrance : Clinical and genetic analysis: Split hand foot malformation

New approaches to fluorescence in situ hybridization

Copy Number Analysis of c- erb -B2 ( HER-2/neu ) and Topoisomerase IIα Genes in Breast Carcinoma by Quantitative Real-Time Polymerase Chain Reaction Using Hybridization Probes and Fluorescence In Situ Hybridization

Copy Number Analysis of c-erb-B2 (HER-2/neu) and Topoisomerase II[alpha] Genes in Breast Carcinoma by Quantitative Real-Time Polymerase Chain Reaction Using Hybridization Probes and Fluorescence In Situ Hybridization

Copy number analysis of c-erb-B2 (HER-2/neu) and topoisomerase IIalpha genes in breast carcinoma by quantitative real-time polymerase chain reaction using hybridization probes and fluorescence in situ hybridization

Loss of Heterozygosity Associated with Uniparental Disomy in Breast Carcinoma

Gene encoding protein elongation factor EEF1A2 is a putative oncogene in ovarian cancer

Protein elongation factor EEF1A2 is a putative oncogene in ovarian cancer

[6] Fluorescence in Situ hybridization of LCM-isolated nuclei from paraffin sections

The retinal rod and cone Na+/Ca2+-K+ exchangers

Laser Capture Microdissection–Guided Fluorescence In Situ Hybridization and Flow Cytometric Cell Cycle Analysis of Purified Nuclei from Paraffin Sections

Hyperthermic induction of premature chromosome condensation in human lymphocytes

Cytogenetic studies in a population suspected to have chromosomal abnormalities

Down syndrome in Ahmedabad: karyotype analysis in 60 cases

Trisomy 21 q: 46,XX,21s+/47,XX,+21q−(q22→qter) mosaicism (de novo) in a down syndrome child

True hermaphrodite: 46, ;XX/46, XY, clinical, cytogenetic and histopathological studies

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