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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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Incidence of Down syndrome in Dubai, UAE

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

2007

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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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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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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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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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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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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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[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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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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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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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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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

Volltextzugriff (PDF)

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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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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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

Volltextzugriff (PDF)

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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Hyperthermic induction of premature chromosome condensation in human lymphocytes

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

1995

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

Incidence of Down syndrome in Dubai, UAE

New approaches to fluorescence in situ hybridization

Loss of Heterozygosity Associated with Uniparental Disomy in Breast Carcinoma

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

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

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

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

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

Protein elongation factor EEF1A2 is a putative oncogene in ovarian cancer

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

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

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

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

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

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

Cytogenetic studies in a population suspected to have chromosomal abnormalities

Down syndrome in Ahmedabad: karyotype analysis in 60 cases

Hyperthermic induction of premature chromosome condensation in human lymphocytes

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

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

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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