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| GUEST EDITORIAL |
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Screening for beta thalassaemia |
p. 1 |
| Mary Petrou |
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| EDITOR’S COMMENTRY |
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Indian Journal of Human Genetics in PubMed: Cautious but confident steps |
p. 6 |
| Kanjaksha Ghosh |
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| ORIGINAL ARTICLES |
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Gly460Trp polymorphism of the ADD1 gene and essential hypertension in an Indian population: A meta-analysis on hypertension risk |
p. 8 |
| P Ramu, G Umamaheswaran, DG Shewade, RP Swaminathan, J Balachander, C Adithan |
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Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India |
p. 16 |
| Nishi Madan, Satendra Sharma, SK Sood, Roshan Colah, HM Bhatia |
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| BRIEF REPORTS |
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Dominant inheritance and intra-familial variations in the association of Sturge-Weber and Klippel-Trenaunay-Weber syndromes |
p. 26 |
| Jose Maria Pereira de Godoy, Agnes Cristina Fett-Conte |
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Heritability estimation of conventional cardiovascular disease risk factors in Asian Indian families: The Calcutta family study |
p. 28 |
| Arnab Ghosh, Rupak Dutta, Angshuman Sarkar |
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| CASE REPORTS |
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Dandy-Walker malformation: An incidental finding |
p. 33 |
| Jyothi Tadakamadla, Santhosh Kumar, GP Mamatha |
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Autism and X-linked hypophosphatemia: A possible association? |
p. 36 |
| Vermeersch Joel, Hellemans Hans, Deboutte Dirk |
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Ataxia telangiectasia: Family management |
p. 39 |
| Arun Seshachalam, Sanju Cyriac, Neelesh Reddy, Sagar T Gnana |
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| LETTER TO EDITOR |
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Glanzmann's thrombasthenia and molecular mimicry |
p. 43 |
| Viroj Wiwanitkit |
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