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TitleDateReferenceAuthorsCall #ISSN
Directing the future of gene therapy in Cyprus: breakthroughs, subjuntivities, and the pragmatics of narrative2018 Cultural anthropology 33 (4): 680-704
  • Theodoros Kyriakides
H6 [CULTURAL-]0886-7356
Inherited blood disorders, genetic risk and global public health: framing 'birth defects' as preventable in India2018 Anthropology and medicine 25 (1): 30-49
  • Sangeeta Chattoo
H6/KGT [BRITISH-]1364-8470in special issue 'Genomics and genetic medicine'
Changes in attitudes towards marriage and reproduction among people with a genetic illness. A study of patients with thalassemia in Iran2017 Anthropology of the Middle East 12 (2): 28-45
  • Sachiko Hosoya
*H6/KW [ANTHRO-]1746-0719in special issue 'Emerging kinship in a changing Middle East'
Anaemia (thalassaemia) in the Middle Euphrates Valley of Syria in the second-fourth centuries AD?2016 Antiquity 90: 157-71
  • Hanna Mańkowska-Pliszka
  • Jacek Tomczyk
  • Krystyna Jędrychowska-Dańska
  • Piotr Palczewski
  • Tomasz Płoszaj
H6/KE [ANTIQUITY-]0003-598X
Choosing offspring: prenatal genetic testing for thalassaemia and the production of a 'saviour sibling' in China2010 Culture, health & sexuality 12 (2): 167-75
  • Margaret Sleeboom-Faulkner
  • Suli Sui
H6/KGT [CULTURE-]1369-1058in special issue 'Quality of offspring - the impact of new reproductive technologies in Asia'; French and Spanish summaries
β-globin gene cluster haplotypes and α-thalassemia in sickle cell disease patients from Trinidad2008 American journal of human biology 20 (3): 342-4
  • Altheia Jones-Lecointe
  • Erskine Smith
  • Marc Romana
  • Marie-Georges Gilbert
  • Waveney P. Charles
H6/HB [AMERICAN-]1042-0533
Infant mortality and reproductive wastage associated with different genotypes of haemoglobinopathies in Orissa, India2007 Annals of human biology 34 (1): 13-25
  • R.S. Balgir
H6/HB [ANNALS-]0301-4460
Consanguinity affects selection of alpha-thalassemia genotypes and the size of populations under selection pressure from malaria2007 Annals of human biology 34 (6): 620-31
  • Chris Frampton
  • M. Gary Nicholls
  • Nicolas Nagelkerke
  • Srdjan Denic
H6/HB [ANNALS-]0301-4460
A study on opportunity of natural selection among the Sindhis of Nagpur city with special reference to beta thalassaemia traits2006 Journal of the Indian Anthropological Society 41 (2): 177-85
  • Kishalaya Das
  • Tapas Kumar Biswas
  • V. R. Rao
H6/KWL [INDIAN-]0019-4387
Implications of the genetic epidemiology of globin haplotypes linked to the sickle cell gene in southern Iran2006 Human biology 78 (6): 719-31
  • Ahmad Merat
  • Nathalie Gerard
  • Rajagopal Krishnamoorthy
  • Ronald L. Nagel
  • Zohreh Rahimi
H6/HB [HUMAN-]0018-7143
The global problem of genetic disease2005 Annals of human biology 32 (2): 117-22
  • D. J. Weatherall
H6/HB [ANNALS-]0301-4460
Alpha-thalassaemia and population health in Southeast Asia2005 Annals of human biology 32 (2): 123-30
  • David K. Chui
H6/HB [ANNALS-]0301-4460German, French, and Spanish summaries
Prevention of thalassaemia and haemoglobinopathies in remote and isolated communities - the Maldives experience2005 Annals of human biology 32 (2): 131-7
  • Naila Firdous
H6/HB [ANNALS-]0301-4460German, French, and Spanish summaries
Establishment of prenatal diagnosis for Beta-thalassaemia: a step towards its control in a developing country2005 Annals of human biology 32 (2): 138-44
  • G. Garewal
  • I. Gupta
  • J. Jaur
  • R. Das
  • R. K. Marwaha
H6/HB [ANNALS-]0301-4460German, French, and Spanish summaries
Genetic disorders in a paediatric hospital in Cambodia2005 Annals of human biology 32 (2): 188-94
  • N. Pises
  • R. Guhadasan
H6/HB [ANNALS-]0301-4460German, French, and Spanish summaries
Occurrence of beta - thalassaemia among the Sindhi community of Jabalpur, Madhya Pradesh (central India)2005 Journal of human ecology 17 (2): 157-8
  • M. P. S. S. Singh
  • N. K. Choudhary
  • P. L. Pande
H6 [JOURNAL-]0970-9274
Beta-globin cluster haplotypes in normal individuals and beta 039-thalassemia carriers from Sardinia, Italy2005 American journal of human biology 17 (6): 765-72
  • A. Falchi
  • G. Vona
  • I. Piras
  • S. Ristaldi
  • V. Latini
H6/HB [AMERICAN-]1042-0533
Origin and expansion of four different beta globin mutations in a single Arab village2005 American journal of human biology 17 (5): 659-61
  • Dori Filon
  • Joël Zlotogora
  • Luci Zalman
  • Saleh Barges
  • Yasir Hujerat
H6/HB [AMERICAN-]1042-0533
Is cribra orbitalia synonymous with anaemia ? Analysis and interpretation of cranial pathology in Sudan2004 American journal of physical anthropology 123 (4): 333-9
  • Eric Grubézy
  • Michael Schultz
  • Ulrike Wapler
H6/HB [AMERICAN-]0002-9483
Blood groups, hemoglobinopathy and G-6-PD deficiency investigations among fifteen major scheduled tribes of Orissa, India2004 The Anthropologist 6 (1): 69-75
  • B. Murmu
  • B. P. Dash
  • R. S. Balgir
H6/HB [ANTHROPOLOGIST, THE: INTERNATIONAL JOURNAL OF CONTEMPORARY AND APPLIED SCIENCES OF MAN-]0972-0073
Paleopathology and dental maturation about neolithic and protohistoric children in France2003 Biométrie humaine et anthropologie 21 (3-4): 285-99
  • E. Peyre
  • J. Granat
H6/HB [BIOTYPOLOGIE-]1279-7863English summary
Beta thalassemia in Nagpur City: a proposed protocol from preventive measeure2002 Man in India 82 (1/2): 117-31
  • Kishalaya Das
  • Ravi A. Wankhede
Characteristic on genetic epidemiology of Chinese Silk Road region2001 Acta anthropologica sinica 20 (1): 69-75
  • Chou Dong-hui
  • Li Hou-jun
  • Li Li
  • Yu Wu-zhong
  • Zhang Yu-hong
1000-3193English summary
Incidence of NESTROFT-positives among the Kolams of district Adilabad, Andhra Pradesh2001 The Anthropologist 3 (3): 207-9
  • A. K. Kalla
  • A. M. Elizabeth
  • K. N. Saraswathy
  • M. P. Sachdeva
  • T. S. Rao
0972-0073
History and orgin of Beta-Thalassemia in Turkey: sequence haplotype diversity of Beta-globin genes2001 Human biology 73 (5): 661-74
  • A. Nazli Başak
  • Gazi Omar Tadmouri
  • Jocelyne Demont
  • Nathalie Garguier
  • Pascale Perrin
0018-7143
B-globin gene haplotypes and a-thalassemia analysis in Babinga pygmies from Congo-Brazzaville2000 Human biology 72 (2): 379-83
  • Didier Montagne Boungou Mpelé
  • Frédéric Galactéros
  • Jean-Marie Bodo
  • Josue Feingold
  • Rene Mouélé
0018-7143
Interaction of different hemoglobinopathies in eastern India with a view to establish genotype-phenotype correlation2000 American journal of human biology 12 (4): 454-9
  • Bani Sengupta
  • Dilip Kumar Bhattacharya
  • Madhusnata De
  • Nikilesh Das
  • Swapan Kumar Das
1042-0533
Past malaria, thalassemia and woman fertility in southern Italy1999 Annals of human biology 26 (2): 163-73
  • A. Degioannis
  • A. Lisa
  • A. Tagarelli
  • G. Zei
  • P. Astolfi
French and German summaries
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
  • M. E. Danubio
0301-4460French and German summaries
Resistance to Falciparum malaria in thalassemia, oxidative stress, and hemoglobin oxidation1999 American journal of physical anthropology 109 (2): 269-73
  • Giovanni Destro-Bisol
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
  • Abdullah Kutlar
  • Ferdane Kutlar
  • Ghazi Omar Tadmouri
  • Onur Bilenoğlu
  • Rhea-Beth Markowitz
Physique in Thalassaemia major1998 Anthropologiai közlemények 39 (1/2): 137-45
  • P Sarkar
  • R. Gaur
H6/HB [ANTHROPOLOGIAI-]0003-5440
Finger and palmar dermatoglyphics of thalassemia patients1998 Man in India 78 (1/2): 135-44
  • A. K. Kapoor
Population screening for B-thalassemia carrier status: evaluation of NESTROFT as a primary screening test1997 Journal of the Anthropological Survey of India 46 (2): 79-90
  • J. Sreenath
  • P. Dhar
  • P. Gangopadhyay
  • V. R. Rao
  • V. R. Tawani
0970-3411
The origin of HbS in Sicily: a toponymic study1993 Human evolution 8 (1): 33-42
  • I Barrai
Rapid and direct detection of the most frequent Mediterranean and -thalassemic mutations by multiplex allele-specific enzymatic amplification1992 Human biology 64 (1): 107-13
  • T Bienvenu
A novel -32(C-A) mutant identified in amplified genomic DNA of a Chinese β -thalassemic patient1992 American Journal of human genetics 50 (1): 237-8
  • Liang-in Lin
Molecular characterization of and -thalassemia in the Sardinian population1992 American Journal of human genetics 50 (2): 422-6
  • M C Rosatelli
Deletional types of alpha-thalassaemia in central Java1992 Human heredity 42 (5): 289-92
  • J A M A Tan