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| EDITORIAL |
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Bombay phenotype in Orissa: What could we make out of it? |
p. 79 |
| Ghosh Kanjaksha, Vasantha K |
| [ABSTRACT] [FULL TEXT] [PDF] |
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| REVIEW ARTICLES |
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Coagulation disorders seen through the window of molecular biology |
p. 81 |
| Ghosh Kanjaksha |
| [ABSTRACT] [FULL TEXT] [PDF] |
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DNA profiling: Social, legal, or biological parentage |
p. 88 |
| Sharma AK |
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| COMMENTARY |
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Can parallel mutation and neutral genome selection explain Eastern African M1 consensus HVS-I motifs in Indian M haplogroups |
p. 93 |
| Winters Clyde |
| [ABSTRACT] [FULL TEXT] [PDF] |
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| ORIGINAL ARTICLES |
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PvuII polymorphism of estrogen receptor-α gene in breast cancer |
p. 97 |
| Surekha D, Vishnupriya S, Rao D Nageswara, Sailaja K, Raghunadharao D |
| [ABSTRACT] [FULL TEXT] [PDF] |
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Possible risk factors for Down syndrome and sex chromosomal aneuploidy in Mysore, South India |
p. 102 |
| Malini Suttur S, Ramachandra Nallur B |
| [ABSTRACT] [FULL TEXT] [PDF] |
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Identification of a rare blood group, "Bombay (Oh) phenotype," in Bhuyan tribe of Northwestern Orissa, India |
p. 109 |
| Balgir RS |
| [ABSTRACT] [FULL TEXT] [PDF] |
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| SHORT ARTICLE |
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Emergence of an unrelated highly aberrant clone in an AML patient at relapse four months after peripheral blood stem cell transplantation |
p. 114 |
| Kadam Pratibha S. Amare, Jain Hemani V, Parikh Purvish M, Saikia Tapan K, Agarwal Sandhya, Ambulkar Indu |
| [ABSTRACT] [FULL TEXT] [PDF] |
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| CASE REPORTS |
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Rett syndrome molecular diagnosis and implications in genetic counseling |
p. 119 |
| Noruzinia M, Akbari MT, Ghofrani M, Sheikhha H |
| [ABSTRACT] [FULL TEXT] [PDF] |
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Mowat-Wilson syndrome in a Moroccan consanguineous family |
p. 122 |
| Ratbi Ilham, Elalaoui Chafai Siham, Dastot-Le Moal Florence, Goossens Michel, Giurgea Irina, Sefiani Abdelaziz |
| [ABSTRACT] [FULL TEXT] [PDF] |
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| LETTER TO THE EDITOR |
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Translocation t(2;14)(p13;q32) in a case of Ph+ acute lymphoblastic leukemia |
p. 125 |
| Kerketta Lily, Vundinti Babu Rao, Ghosh Kanjaksha |
| [ABSTRACT] [FULL TEXT] [PDF] |
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