Preface iii

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Anupam Kaur and Jai Rup Singh • Chromosomal Abnormalities: Genetic Disease Burden in India

1-14

DOI: 10.31901/24566330.2010/10.1-3.01

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Prochi F. Madon, Arundhati S. Athalye, Kunal Sanghavi and Firuza R. Parikh • Microdeletion Syndromes Detected by FISH – 73 Positive from 374 Cases

15-20

DOI: 10.31901/24566330.2010/10.1-3.02

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Usha Dave and Dhanlaxmi Shetty • Chromosomal Abnormalities in Mental Retardation:  Indian Experience

21-32

DOI: 10.31901/24566330.2010/10.1-3.03

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G. K. Chetan, K. R. Manjunatha, H. N. Venkatesh, S. Balu, E. Venkataswamy  and S. Roy • Cytogenetic Studies of Idiopathic Mental Retardation: A Report

33-39

DOI: 10.31901/24566330.2010/10.1-3.04

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Parvinder Kumar, Ashma Gupta, Roopali Fotra, Upma, Sunil Raina, Surbhi Sethi, T.R.Raina and Subash Gupta • Chromosomal Anomalies in Referred Cases with Suspected Genetic Disorders: First Report from Jammu and Kashmir

41-47

DOI: 10.31901/24566330.2010/10.1-3.05

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M. Rajasekhar, R. Murugesan, Rekharao, H. Shetty, Jyothirao, P. M. Gopinath and  K. Satyamoorthy  • Cytogenetic Analysis of 1400 Referral Cases: Manipal Experience

49-55

DOI: 10.31901/24566330.2010/10.1-3.06

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Radhakrishnan Yashwanth,  Nallathambi Chandra  and P M. Gopinath • Chromosomal Abnormalities among Children with Congenital Malformations

57-63

DOI: 10.31901/24566330.2010/10.1-3.07

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V. Kalavathi, N. Chandra, G. Renjini Nambiar, Jayashree Shanker,  P. Sugunashankari, J. Meena, T. Jegatheesan, S. T. Santhiya, A. Ramesh, P. M. Gopinath and K. M. Marimuthu • Chromosomal Abnormalities in 979 Cases of Amenorrhea: A Review

65-69

DOI: 10.31901/24566330.2010/10.1-3.08

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J. Vijayalakshmi, Teena Koshy, Harpreet Kaur, F. Andrea Mary, R. Selvi, V. Deepa Parvathi, R. Bhavani, R. Vikram Jayanth, P. Venkatchalam and Solomon F. D. Paul •Cytogenetic  Analysis of Patients with Primary Amenorrhea

71-76

DOI: 10.31901/24566330.2010/10.1-3.09

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M. Margaret, P. Tilak and S. Rajangam • 45,X/47,X,i(X)(q10),i(X)(q10)/46,X,i(X)(q10) Isochromosome Xq in Mosaic Turner syndrome

77-80

DOI: 10.31901/24566330.2010/10.1-3.10

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R. Sangeetha,  V. Balachandar, S. Mohana Devi, P. Velmurugan, B. Lakshman Kumar, P. Manikantan, M. Arun, A. Karthick Kumar, S. Mustaq Ahamed, B. Balamuralikrishnan and K. Sasikala • Cytogenetic Study on Sexual Ambiguity in Humans

81-86

DOI: 10.31901/24566330.2010/10.1-3.11

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N. Chandra, Cyrus Cyril, Prema Lakshminarayana, P. Nallasivam, A. Ramesh, P. M. Gopinath and K. M. Marimuthu • Cytogenetic Evaluation of Down Syndrome: A Review of 1020 Referral Cases

87-93

DOI: 10.31901/24566330.2010/10.1-3.12

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Jayalakshamma, Mary Margaret, S Amudha, Preetha Tilak, Rema Devi and Sayee Rajangam • Cytogenetic Analysis in Down Syndrome

95-99

DOI: 10.31901/24566330.2010/10.1-3.13

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Radhakrishnan Yashwanth,  Nallathambi Chandra and P. M. Gopinath • Satellite Associations in Down Syndrome  

101-104

DOI: 10.31901/24566330.2010/10.1-3.14

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Suttur S. Malini  and Nallur B. Ramachandra • Young Mothers Produce More Chromosomal Syndrome Babies in Mysore, South India

105-112

DOI: 10.31901/24566330.2010/10.1-3.15

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Preetha Tilak • Effect of Reciprocal Translocations on Phenotypic Abnormalities

113-119

DOI: 10.31901/24566330.2010/10.1-3.16

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Abdul Vahab Saadi, Pralhad Kushtagi, PM Gopinath and Kapaettu Satyamoorthy • Quantitative Fluorescence Polymerase Chain Reaction (QF-PCR) for Prenatal Diagnosis of Chromosomal Aneuploidies

121-129

DOI: 10.31901/24566330.2010/10.1-3.17

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Smitha Rame Gowda, Harshavardhan M. Gawde, Abbas Hyderi, Mysore R. Savitha, Balasundaram Krishnamurthy, Sameul C. Karat, Narayanappa Doddaiah, Zareen M. Patel and Nallur B Ramachandra • Chromosomal Anomalies and Congenital Heart Disease in Mysore, South India

131-139

DOI: 10.31901/24566330.2010/10.1-3.18

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B. Lakshman Kumar, V. Balachandar, K. Suresh, R. Sangeetha, S. Mohana Devi and K. Sasikala  • Tropical Chronic Pancreatitis (TCP): A Cytogenetic Study in Patients Residing in and around Coimbatore City, Tamil Nadu

141-145

DOI: 10.31901/24566330.2010/10.1-3.19

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Kamlesh Guleria and Vasudha Sambyal • Spectrum of Chromosomal Aberrations in Peripheral Blood Lymphocytes of Gastrointestinal Tract (GIT) and Breast Cancer Patients

147-158

DOI: 10.31901/24566330.2010/10.1-3.20

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V. Balachandar, B. Lakshman Kumar, S. Mohana Devi, R. Sangeetha, P. Manikantan, S. Suresh Kumar, S. Sudha, K. Sasikala and S.N. Dharwatgar • Identification of Chromosome Aberrations among Benign Prostatic Hyperplasia Patients in Tamilnadu, Southern India

159-164

DOI: 10.31901/24566330.2010/10.1-3.21

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Radhakrishnan Yashwanth,  Nallathambi Chandra, Palliath Mohandas and Puthiya M. Gopinath • Urofacial (Ochoa) Syndrome - A Case Report

165-168

DOI: 10.31901/24566330.2010/10.1-3.22

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V.G. Abilash, Radha Saraswathyand K.M. Marimuthu • Inter Chromosomal Effect (ICE) Resulting in Increased Abnormal Pregnancies in an Infertile Female with a Rare Robertsonian Translocation (13;21)(p10;p10) and SRY Gene carrier with 9 Consecutive Abortions

169-174

DOI: 10.31901/24566330.2010/10.1-3.23

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J. Gazala, I. V. Amithkumar, J. Sabina, K.K. Praveena and J. Sujatha • Prenatal Diagnosis in Pericentric Inversion 6

175-178

DOI: 10.31901/24566330.2010/10.1-3.24

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A. Venkateshwari, Ashrafunnisa Begum, A. Srilekha M. Sujatha Pratibha Nallari and A. Jyothy • A 21/22 Translocation in a Female with Repeated Abortions: A Case Report

179-181

DOI: 10.31901/24566330.2010/10.1-3.25

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Angel  Beula P.R, Sridevi Hegde, Priti Venkatesh and Jayaprakash • Evaluation of Cardiac Defect in a Fetus with 8p Interstitial Deletion

183-186

DOI: 10.31901/24566330.2010/10.1-3.26

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Jai Rup Singh, Arvind Rup Singh and Arsh Rup Singh • Directory of Human Genetic Services in  India – 2007

187-192

DOI: 10.31901/24566330.2010/10.1-3.27

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Guide to Contributors

193-200

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List of Members of the Editorial Board

201-206

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VOLUME 10, Number 4                                                                                                                                         DECEMBER , 2010

Vandana Rai • Autism Susceptibility Genes Identification by Linkage Analysis: A Review

207-216

DOI: 10.31901/24566330.2010/10.04.01

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Barbara Busert, Gesa Schwanitz, Regine Schubert, Ulrike Gamerdinger and Ingo G.H Schmidt-Wolf • Characterization of the Karyotype in Patients with Multiple Myeloma by the Combination of Karyotype Analysis, FISH and CGH

217-222

DOI: 10.31901/24566330.2010/10.04.02

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Ariz Akhter, Vinita Das, Amita Pandey and Suraksha Agrawal •  Effect of Glucocorticoids on Transcriptional Status of HLA-G in Human Trophoblast Cells from Full Term Placenta

223-229

DOI: 10.31901/24566330.2010/10.04.03

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Mutlu Karkucak, Sebnem Sag, Tahsin Yakut and Yalcin Kimya •  Prenatal Diagnosis of De Novo Reciprocal Translocation  t(1;12)(q21.3;p11.2)  with Trisomy 21 and Sperm FISH  Analysis for Increased Aneuploidy Risk

231-234

DOI: 10.31901/24566330.2010/10.04.04

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M. Veronica, Altaf Ali, A. Venkateshwari, C. Narsimhan and  Pratibha Nallari •  AAT: A Comparative Study in HCM and DCM

235-238

DOI: 10.31901/24566330.2010/10.04.05

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Pankaj K. Gadhia, Rahul P. Thumbar and Bhavesh Kevadiya •  Cytome Assay of Buccal Epithelium for Bio-monitoring Genotoxic Assessment of Benzene Exposure among Petrol Pump Attendants

239-245

DOI: 10.31901/24566330.2010/10.04.06

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Sonali Paul and Madhusnata De •  Changes in Anti-Oxidant Enzyme Profile during Haematological Malignancy

247-250

DOI: 10.31901/24566330.2010/10.04.07

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Munisamy Anbazhagan, Ponnan Arumugam,  Arabandi Ramesh and Sathiyavedu Thyagarajan Santhiya •  Genetic Risk Assessment in Traffic Policemen of Chennai City by Sister Chromatid Exchange Analysis

251-255

DOI: 10.31901/24566330.2010/10.04.08

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Sikta Bandopadhyay,  Nirmal K. Bera,  Chitta R. Nayak, and Tapas Kumar Chaudhuri   •  Dopamine Receptor Gene D1 Reveals No Significant Association with Delusional Disorder on the Basis of Ssp Analysis

257-261

DOI: 10.31901/24566330.2010/10.04.09

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Pankaj Gadhia, Sumitra Chakraborty and Meonis Pithawala • Cytogenetic Studies on Railway Engine Drivers Exposed to Extremely Low Frequency Electromagnetic Fields (ELF-EMF)

263-269

DOI: 10.31901/24566330.2010/10.04.10

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Index 

271-274

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