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VOLUME 9 CONTENTS 2009 |
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VOLUME 9, Number 1 MARCH, 2009 |
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Annegret Geipel, Thomas Eggermann, Gisela Knöpfle, Gesa Schwanitz, Ursula Pätzold and Dagmar Hansmann • Non-Mosaic Trisomy 7 in Chorionic Villi and Trisomy 18 in the Fetus: An Extreme form of Mosaic Variegated Aneuploidy? 1-4
N. Subramanian, H. Mohana Krishnan, P. Venkatachalam and P.A.C. Kamatchi • A Study of Lactate Dehydrogenase (LDH) Isoenzyme is a Biochemical Tumour Marker in Cervical Carcinoma Patients 5-12
M. Karthikeyan, Rajiv Rose, V. Shridevi, B. Anandan, S. Shanmugasundaram, D. Mohan, A. Ramesh and G. Jayaraman • Core Promoter Variants (A-20C, T-18C and G-6A) of the Angiotensinogen (AGT) Gene are not Significantly Associated with Hypertension in Patients of Tamilnadu, 13-19
Pushpa Saviour, Prakash Padakannaya, Surendranath Nishanimutt and Nallur B. Ramachandra • Familial Patterns and Biological Markers of Dyslexia 21-29
Valentina I. Rykova , Galina M. Ronichevskaya and Elvira V. Grigorieva • Effect of Total Proteoglycans on Cell Proliferation and Tumor Formation in Mice 31-37
A.I. Ibraimov • Noncoding Dnas and Origin of Sex 39-47
Tabrez Jafar, Gaurav Tripathi, Abass A. Mehndi, Kaushik Mandal, Sanjeev Gulati, Raj K Sharma, Vinod P. Baburaj, Shaily Awasthi and Suraksha Agrawal • Vitamin D Receptor Gene Polymorphisms in Indian Children with Idiopathic Nephrotic Syndrome 49-55
Guide to Contributors 57-62
List of Members of the Editorial Board 63-68
VOLUME 9, Number 2 JUNE, 2009
G. Gandhi and Gunjan • Exercise-Induced Genetic Damage: A Review 69-96
Vipin Gupta, K. N. Saraswathy, Rajesh Khadgawat and M. P. Sachdeva • Genome-wide Association: “A Revolutionary Approach” 97-103
Minakshi Vashist, Neelkamal, Ritu Yadav and Meena Lal • Trisomy - T(21;21) with mosaicisim in a Down Syndrome Girl Child Case Report 105-107
B. Ushasree, S. Yasmeen, A. Venkateshwari, C. Narsimhan, R. K. Jain and Pratibha Nallari • Association of Polymorphic Antioxidant Enzymes with Dilated Cardiomyopathy 109-113
Zahra Fazeli and Sadeq Vallian • Estimation Haplotype Frequency of BglII/EcoRI/VNTR Markers at the PAH Gene Region in Iranian Population 115-121
M. Eunice, B. Kulshreshtha, A. Kriplani, Rima Dada, S. Agarwal S, K. Kucheria, A. K. Karak, S. Datta Gupta and A. C. Ammini • Familial Pure Gonadal Dysgenesis with 46, XY Karyotype in Three Siblings and Gonadoblastoma in the Youngest Sibling 123-126
U. Shankarkumar, V. D. Pradhan, M. Patwardhan, A.Pawar, A.Almeida and K Ghosh • HLA Alleles in Anti-Endothelial Cell Antibody Positive Indian SLE Patients 127-130
Sujana Katta, Shivani Vadapalli, R.Sushant, B. K. S. Sastry and Pratibha Nallari • Genetic Markers in Idiopathic Pulmonary Arterial Hypertension (IPAH) 131-137
Priya A. Iyer, Jaya C. Vyas, Prabhat Ranjan and Dhananjaya Saranath • A de novo Complex Chromosomal Rearrangement of 46,XX,t(7;15;13)(p15;q21;q31) in a Female with an Adverse Obstetric History 139-143
VOLUME 9, Number 3-4 SEPTEMBER-DECEMBER, 2009
M. K. Bhasin • Morphology to Molecular Anthropology: Castes and Tribes of India 145-230
Badaruddoza, A.J.S. Bhanwer, R. Sawhney, N.K. Randhawa, K. Matharoo and B. Barna • A Study of Angiotensin Converting Enzyme (ACE) Gene Polymorphism in Essential Hypertension among a Business Community in Punjab 231-234
Ranganath Vallabhajosyula, Preetha Tilak and Sayee Rajangam • Ring chromosome 21: A Case Report 235-238
Khalid Sadki, Hoda Lamsyah, Blanca Rueda, Ouafae Lahlou, Rajae El Aouad and Javier Martin • Cd209 Promoter Single Nucleotide Polymorphism -336a/G and the Risk of Susceptibility to Tuberculosis Disease in the Moroccan Population 239-243
Bisu Singh, Ganesh Chandra Mallick, Sikta Bandopadhyay, Chitta R. Nayak and Tapas Kumar Chaudhuri • Study of Selected HLA-A and -B Antigens by PCR-SSP Method in Bengali Population of Siliguri and Adjoining Areas of West Bengal 245-249
K. S. Santhy, Anupama, M. Srividya, K.S. Mangayarkarasi, P. Arulraj and M.V. Usharani • Assessment of Tumour Response to Multimodalities of Treatment in Locally Advanced Breast Cancer Patients Using Comet Assay 251-254
Metin Demirkaya, Betül Sevinir, Yakup Canitez, Özlem Bostan and Meral Yildiz • A Case with the Combination of Bilateral Microphthalmia, Unilateral Pulmonary Agenesis, Diaphragmatic Eventration and Atrial Septal Defect: PDAC Syndrome 255-261
Matsa Lova Satyanarayana, Rangaraju Advithi, Ananthapur Venkateshwari and Pratibha Nallari • Pro and Anti-Oxidants in Cardiomyopathy 263-267
Magdalena Gogiel, Sabrina Spengler, Isabelle Leisten, Nadine Schönherr, Gesa Schwanitz, Alina T. Midro, Gerhard Binder and Thomas Eggermann • Molecular Analyses of the Boris Gene in Children with Silver-Russell Syndrome 269-272
Information 273-274
Index 275-277
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