Title | Date | Reference | Authors | Call # | ISSN | ||
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Screening of possible Beta-thalassemia amongst the Ahir community of Delhi and NCR | 2024 | International journal of anthropology 39 (3-4): 285-92 | H6/HB [INTERNATIONAL-] | 0393-9383 | |||
Possible thalassemia intermedia in a child (16th-18th century) from the westernmost part of Europe: potential association with malaria and past migrations | 2024 | Anthropological Science 132 (2): 133-42 | H6/KWV [ZINRUIGAKU-] | 0918-7960 | |||
Assessment of knowledge, attitude and practice toward Beta-thalassemia among Ahir community in Delhi and NCR | 2024 | International journal of anthropology 39 (3-4): 273-83 | H6/HB [INTERNATIONAL-] | 0393-9383 | |||
Beta thalassemia trait: current status in India | 2023 | International journal of anthropology 38 (3-4): 203-15 | H6/HB [INTERNATIONAL-] | 0393-9383 | |||
Directing the future of gene therapy in Cyprus: breakthroughs, subjuntivities, and the pragmatics of narrative | 2018 | Cultural anthropology 33 (4): 680-704 | H6 [CULTURAL-] | 0886-7356 | |||
Inherited blood disorders, genetic risk and global public health: framing 'birth defects' as preventable in India | 2018 | Anthropology and medicine 25 (1): 30-49 | H6/KGT [BRITISH-] | 1364-8470 | |||
Changes in attitudes towards marriage and reproduction among people with a genetic illness. A study of patients with thalassemia in Iran | 2017 | Anthropology of the Middle East 12 (2): 28-45 | *H6/KW [ANTHRO-] | 1746-0719 | |||
Anaemia (thalassaemia) in the Middle Euphrates Valley of Syria in the second-fourth centuries AD? | 2016 | Antiquity 90 (): 157-71 | H6/KE [ANTIQUITY-] | 0003-598X | |||
Choosing offspring: prenatal genetic testing for thalassaemia and the production of a 'saviour sibling' in China | 2010 | Culture, health & sexuality 12 (2): 167-75 | H6/KGT [CULTURE-] | 1369-1058 | |||
Mutações genéticas humanas e fluxos populacionais - Portugal e o Mediterrâneo | 2010 | Trabalhos de antropologia e etnologia 50 (): 113-20 | H6/KVE [SOCIEDADE-] | ||||
β-globin gene cluster haplotypes and α-thalassemia in sickle cell disease patients from Trinidad | 2008 | American journal of human biology 20 (3): 342-4 | H6/HB [AMERICAN-] | 1042-0533 | |||
Consanguinity affects selection of alpha-thalassemia genotypes and the size of populations under selection pressure from malaria | 2007 | Annals of human biology 34 (6): 620-31 | H6/HB [ANNALS-] | 0301-4460 | |||
Infant mortality and reproductive wastage associated with different genotypes of haemoglobinopathies in Orissa, India | 2007 | Annals of human biology 34 (1): 13-25 | H6/HB [ANNALS-] | 0301-4460 | |||
Implications of the genetic epidemiology of globin haplotypes linked to the sickle cell gene in southern Iran | 2006 | Human biology 78 (6): 719-31 | H6/HB [HUMAN-] | 0018-7143 | |||
A study on opportunity of natural selection among the Sindhis of Nagpur city with special reference to beta thalassaemia traits | 2006 | Journal of the Indian Anthropological Society 41 (2): 177-85 | H6/KWL [INDIAN-] | 0019-4387 | |||
Genetic disorders in a paediatric hospital in Cambodia | 2005 | Annals of human biology 32 (2): 188-94 | H6/HB [ANNALS-] | 0301-4460 | |||
The global problem of genetic disease | 2005 | Annals of human biology 32 (2): 117-22 | H6/HB [ANNALS-] | 0301-4460 | |||
Alpha-thalassaemia and population health in Southeast Asia | 2005 | Annals of human biology 32 (2): 123-30 | H6/HB [ANNALS-] | 0301-4460 | |||
Prevention of thalassaemia and haemoglobinopathies in remote and isolated communities - the Maldives experience | 2005 | Annals of human biology 32 (2): 131-7 | H6/HB [ANNALS-] | 0301-4460 | |||
Origin and expansion of four different beta globin mutations in a single Arab village | 2005 | American journal of human biology 17 (5): 659-61 | H6/HB [AMERICAN-] | 1042-0533 | |||
Beta-globin cluster haplotypes in normal individuals and beta 039-thalassemia carriers from Sardinia, Italy | 2005 | American journal of human biology 17 (6): 765-72 | H6/HB [AMERICAN-] | 1042-0533 | |||
Occurrence of beta - thalassaemia among the Sindhi community of Jabalpur, Madhya Pradesh (central India) | 2005 | Journal of human ecology 17 (2): 157-8 | H6 [JOURNAL-] | 0970-9274 | |||
Establishment of prenatal diagnosis for Beta-thalassaemia: a step towards its control in a developing country | 2005 | Annals of human biology 32 (2): 138-44 | H6/HB [ANNALS-] | 0301-4460 | |||
Blood groups, hemoglobinopathy and G-6-PD deficiency investigations among fifteen major scheduled tribes of Orissa, India | 2004 | The Anthropologist 6 (1): 69-75 | H6/HB [ANTHROPOLOGIST, THE: INTERNATIONAL JOURNAL OF CONTEMPORARY AND APPLIED SCIENCES OF MAN-] | 0972-0073 | |||
Is cribra orbitalia synonymous with anaemia ? Analysis and interpretation of cranial pathology in Sudan | 2004 | American journal of physical anthropology 123 (4): 333-9 | H6/HB [AMERICAN-] | 0002-9483 | |||
Paleopathology and dental maturation about neolithic and protohistoric children in France | 2003 | Biométrie humaine et anthropologie 21 (3-4): 285-99 | H6/HB [BIOTYPOLOGIE-] | 1279-7863 | |||
Beta thalassemia in Nagpur City: a proposed protocol from preventive measeure | 2002 | Man in India 82 (1/2): 117-31 | |||||
History and orgin of Beta-Thalassemia in Turkey: sequence haplotype diversity of Beta-globin genes | 2001 | Human biology 73 (5): 661-74 | 0018-7143 | ||||
Incidence of NESTROFT-positives among the Kolams of district Adilabad, Andhra Pradesh | 2001 | The Anthropologist 3 (3): 207-9 | 0972-0073 | ||||
Characteristic on genetic epidemiology of Chinese Silk Road region | 2001 | Acta anthropologica sinica 20 (1): 69-75 | 1000-3193 | ||||
B-globin gene haplotypes and a-thalassemia analysis in Babinga pygmies from Congo-Brazzaville | 2000 | Human biology 72 (2): 379-83 | 0018-7143 | ||||
Interaction of different hemoglobinopathies in eastern India with a view to establish genotype-phenotype correlation | 2000 | American journal of human biology 12 (4): 454-9 | 1042-0533 | ||||
Resistance to Falciparum malaria in thalassemia, oxidative stress, and hemoglobin oxidation | 1999 | American journal of physical anthropology 109 (2): 269-73 | H6/HB [AMERICAN-] | ||||
Identification of the Chinese IVS-II-654 (C→T) b-thalassemia mutation in an immigrant Turkish family: recurrence or migration? | 1999 | Human biology 71 (2): 295-302 | |||||
Endogamy and inbreeding since the 17th century in past malarial communities in the province of Consenza (Calabria, southern Italy) | 1999 | Annals of human biology 26 (5): 473-88 | 0301-4460 | ||||
Past malaria, thalassemia and woman fertility in southern Italy | 1999 | Annals of human biology 26 (2): 163-73 | |||||
Finger and palmar dermatoglyphics of thalassemia patients | 1998 | Man in India 78 (1/2): 135-44 | |||||
Physique in Thalassaemia major | 1998 | Anthropologiai közlemények 39 (1/2): 137-45 | H6/HB [ANTHROPOLOGIAI-] | 0003-5440 | |||
Population screening for B-thalassemia carrier status: evaluation of NESTROFT as a primary screening test | 1997 | Journal of the Anthropological Survey of India 46 (2): 79-90 | 0970-3411 | ||||
The origin of HbS in Sicily: a toponymic study | 1993 | Human evolution 8 (1): 33-42 | |||||
Deletional types of alpha-thalassaemia in central Java | 1992 | Human heredity 42 (5): 289-92 | |||||
Molecular characterization of and -thalassemia in the Sardinian population | 1992 | American Journal of human genetics 50 (2): 422-6 | |||||
A novel -32(C-A) mutant identified in amplified genomic DNA of a Chinese β -thalassemic patient | 1992 | American Journal of human genetics 50 (1): 237-8 | |||||
Rapid and direct detection of the most frequent Mediterranean and -thalassemic mutations by multiplex allele-specific enzymatic amplification | 1992 | Human biology 64 (1): 107-13 |