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Hindi Relevant Articles [224]
Research Article
Occurrence of Chromosomal Alterations in Recurrent Spontaneous Abortion Couples: A Case-Only Study from Kashmir, North India
Mahrukh H Zargar, Tahir M Malla and Fayaz A Dar
Case Report
Unusual Hairy Projections in a Case of T-acute Lymphoblastic Leukemia, a Cause for Diagnostic Dilemma: A Case Report
Venkatesan Somasundaram, Ankur Ahuja, Prabhu Manivannan, Dinesh Chandra, Abhishek Purohit and Renu Saxena
Research Article
Autosomal Dominant Corneal Dystrophy with TGFBI Mutations: Lessons Learned from a Chinese Pedigree
Anli Shu, Zheng Wei, Yibin Hao, Hai Luo, Fu Tian, Fred G Biddle, Wei Wu, Min Liu and Wei Cao
Research Article
Variation in Milk Yield, Contents and Incomes According to Somatic Cell Count in a Large Dairy Goat Population
Francisco Javier Pleguezuelos, Luis Fernando De La Fuente and Carlos Gonzalo
Research Article
Assessment of Cattle Fattening and Marketing Practice in Harshin District of Somali Regional State, Ethiopia
Sisay Fikru
Research Article
Effect of Regular Physical Activity on Metabolic Control in Pediatric Age Group with Type 1 Diabetes Mellitus
Abdulmoein E Al-Agha, Somayah I Alrefaie, Ihab Abd elhameed Ahmed and Douaa Ahmed El Derwi
Research Article
Combinatorial Efficacy of Nanoliposomal Ceramide and the Antioxidant 7,8- Benzoflavone for Acute Myeloid Leukemia
Brian M. Barth, Timothy J. Brown, Matthew T. Adams, Aileen M. Garcia, Lindsey N. Fisher, Jennifer L. Fritz, Adam J. Beck, Colin M. McGill, Mark Kester, Melissa A. Tran and David F. Claxton
Research Article
Autosomal Dominant Hereditary Essential Thrombocythemia due to a Gain of Function Mutation in the Thrombopoietin (TPO) and JAK2 Gene as the Cause of Congenital Aspirin-Responsive Sticky Platelet Syndrome: Personal Experiences and Review of the Litera
Jan Jacques Michiels, Jan Stasko, Peter Kubish, Achille Pich and Hendrik De Raeve
Short Communication
Considerations to Calculate Expected Genotypic Frequencies and Formal Statistical Testing of Hardy-Weinberg Assumptions for nonpseudoautosomal X chromosome SNPs
Fernando Pires Hartwig