Items where authors include "Jafri, H"

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Number of items: 11.

Article

Ahmed, S orcid.org/0000-0003-4212-0388, Jafri, H, Ahmed, WN et al. (3 more authors) (2023) Pakistani healthcare professionals’ perceptions of communication with patients and their relatives about hereditary breast cancer: a qualitative study in a LMIC. Journal of Community Genetics, 14. pp. 287-294. ISSN 1868-310X

Panagiotou, ES, Fernandez-Fuentes, N, Farraj, LA et al. (10 more authors) (2022) Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia. Molecular Vision, 28. pp. 57-69. ISSN 1090-0535

Ahmed, S orcid.org/0000-0003-4212-0388, Jafri, H, Faran, M et al. (4 more authors) (2022) Cascade screening for beta-thalassaemia in Pakistan: relatives’ experiences of a decision support intervention in routine practice. European Journal of Human Genetics, 30 (4). pp. 406-412. ISSN 1018-4813

Ahmed, S orcid.org/0000-0003-4212-0388, Jafri, H, Rashid, Y et al. (3 more authors) (2021) Cascade screening for beta-thalassemia in Pakistan: development, feasibility and acceptability of a decision support intervention for relatives. European Journal of Human Genetics, 30. pp. 73-80. ISSN 1018-4813

Dong, D, Ahmed, S orcid.org/0000-0003-4212-0388, Nichini, E et al. (5 more authors) (2021) Decision making on antenatal screening results: A comparative Q-method study of women from two Chinese cities. Health Expectations, 24 (2). pp. 363-376. ISSN 1369-6513

Ahmed, S orcid.org/0000-0003-4212-0388, Jafri, H, Rashid, Y et al. (4 more authors) (2019) Autonomous decision-making for antenatal screening in Pakistan: views held by women, men and health professionals in a low–middle income country. European Journal of Human Genetics, 27. pp. 848-856. ISSN 1018-4813

Ahmed, S orcid.org/0000-0003-4212-0388, Yi, H, Dong, D et al. (5 more authors) (2018) Interpretations of autonomous decision-making in antenatal genetic screening among women in China, Hong Kong and Pakistan. European Journal of Human Genetics, 26 (4). pp. 495-504. ISSN 1018-4813

Ahmed, S, Jafri, H, Rashid, Y et al. (3 more authors) (2017) Attitudes towards non-invasive prenatal diagnosis among obstetricians in Pakistan: a developing, Islamic country. Prenatal Diagnosis, 37 (3). pp. 289-295. ISSN 0197-3851

Parry, DA, Smith, CEL orcid.org/0000-0001-8320-5105, El-Sayed, W et al. (17 more authors) (2016) Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta. American Journal of Human Genetics, 99 (4). pp. 984-990. ISSN 0002-9297

Khan, K, Logan, CV, McKibbin, M et al. (18 more authors) (2012) Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects. Human Molecular Genetics, 21 (4). pp. 776-783. ISSN 0964-6906

Bryant, LD orcid.org/0000-0002-1972-7395, Ahmed, S orcid.org/0000-0003-4212-0388, Ahmed, M et al. (2 more authors) (2011) 'All is done by Allah'. Understandings of Down syndrome and prenatal testing in Pakistan. Social Science & Medicine, 72 (8). pp. 1393-1399. ISSN 0277-9536

This list was generated on Sat Mar 23 23:26:13 2024 GMT.