Works matching Hemophilia and genetics
Results: 425
Genetic variant detection in a South African haemophilia B population.
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- Haemophilia, 2024, v. 30, n. 3, p. 765, doi. 10.1111/hae.14978
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- Article
Accessibility and visibility of genetic testing for haemophilia across Europe: Where do we stand?
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- Haemophilia, 2023, v. 29, n. 1, p. 256, doi. 10.1111/hae.14672
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- Article
Genetic causes of haemophilia in women and girls.
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- Haemophilia, 2021, v. 27, n. 2, p. e164, doi. 10.1111/hae.14186
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- Article
Inhibitor epidemiology and genetic‐related risk factors in people with haemophilia from Côte d'Ivoire.
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- Haemophilia, 2020, v. 26, n. 1, p. 79, doi. 10.1111/hae.13902
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- Article
'Just an unfortunate coincidence': children's understanding of haemophilia genetics and inheritance.
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- Haemophilia, 2011, v. 17, n. 3, p. 470, doi. 10.1111/j.1365-2516.2010.02448.x
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- Article
Attitudes towards and beliefs about genetic testing in the haemophilia community: a qualitative study.
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- Haemophilia, 2007, v. 13, n. 5, p. 633, doi. 10.1111/j.1365-2516.2007.01454.x
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- Article
Genetic services available for counselling and prenatal diagnosis of haemophilia.
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- Haemophilia, 1998, v. 4, p. 24, doi. 10.1046/j.1365-2516.1998.0040s2024.x
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- Article
Exploring Female Relatives of Patients with Hemophilia' Awareness, Attitudes, and Understanding Towards Genetic Testing [Letter].
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- Journal of Multidisciplinary Healthcare, 2024, v. 17, p. 879, doi. 10.2147/JMDH.S464878
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- Article
A Genetic and Demographic Study of Hemophilia A in Brazil.
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- Human Heredity, 1985, v. 35, n. 4, p. 250, doi. 10.1159/000153554
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- Article
Genetic Characteristics of Hemophilia A in Chile.
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- Human Heredity, 1980, v. 30, n. 3, p. 161, doi. 10.1159/000153122
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- Article
Molecular genetics of hemophilia A: Clinical perspectives.
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- Egyptian Journal of Medical Human Genetics, 2010, v. 11, n. 2, p. 105, doi. 10.1016/j.ejmhg.2010.10.005
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- Article
Genetic mosaicism in haemophilia: A practical review to help evaluate the risk of transmitting the disease.
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- Haemophilia, 2020, v. 26, n. 3, p. 375, doi. 10.1111/hae.13975
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- Article
Genetic determinants of immunogenicity to factor IX during the treatment of haemophilia B.
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- Haemophilia, 2015, v. 21, n. 2, p. 210, doi. 10.1111/hae.12553
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- Article
Prenatal diagnosis in haemophilia A: experience of the genetic diagnostic laboratory.
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- Haemophilia, 2014, v. 20, n. 6, p. e384, doi. 10.1111/hae.12517
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- Publication type:
- Article
Genetic factors influencing inhibitor development in a cohort of South African haemophilia A patients.
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- Haemophilia, 2014, v. 20, n. 5, p. 687, doi. 10.1111/hae.12436
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- Publication type:
- Article
F8 haplotype and inhibitor risk: results from the Hemophilia Inhibitor Genetics Study (HIGS) Combined Cohort.
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- Haemophilia, 2013, v. 19, n. 1, p. 113, doi. 10.1111/hae.12004
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- Publication type:
- Article
Genetic polymorphism of IL28B in hepatitis C-infected haemophilia patients in Israel.
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- Haemophilia, 2013, v. 19, n. 1, p. 150, doi. 10.1111/j.1365-2516.2012.02932.x
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- Article
Accurate tracking genetic markers in haemophilia linkage analysis: a matter beyond scientific priority.
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- Haemophilia, 2012, v. 18, n. 4, p. e359, doi. 10.1111/j.1365-2516.2012.02859.x
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- Article
A Modified I-PCR to detect the factor VIII Inv22 for genetic diagnosis and prenatal diagnosis in haemophilia A.
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- Haemophilia, 2012, v. 18, n. 3, p. 452, doi. 10.1111/j.1365-2516.2011.02670.x
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- Publication type:
- Article
Quality and easy availability of medical support overwhelmingly determines the attitude and belief towards genetic testing in haemophilia.
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- 2008
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- Publication type:
- Letter
Genetic diagnosis of haemophilia and other inherited bleeding disorders.
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- Haemophilia, 2006, v. 12, p. 82, doi. 10.1111/j.1365-2516.2006.01263.x
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- Article
A rapid multifluorescent polymerase chain reaction for genetic counselling in Chinese haemophilia A families.
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- Haemophilia, 2006, v. 12, n. 1, p. 62, doi. 10.1111/j.1365-2516.2005.01162.x
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- Article
The molecular analysis of haemophilia A: a guideline from the UK haemophilia centre doctors’ organization haemophilia genetics laboratory network.
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- Haemophilia, 2005, v. 11, n. 4, p. 387, doi. 10.1111/j.1365-2516.2005.01111.x
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- Publication type:
- Article
The molecular analysis of haemophilia B: a guideline from the UK haemophilia centre doctors’ organization haemophilia genetics laboratory network.
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- Haemophilia, 2005, v. 11, n. 4, p. 398, doi. 10.1111/j.1365-2516.2005.01112.x
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- Article
Haemophilia Inhibitor Genetics Study – evaluation of a model for studies of complex diseases using linkage and association methods.
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- Haemophilia, 2005, v. 11, n. 4, p. 427, doi. 10.1111/j.1365-2516.2005.01119.x
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- Article
A framework for genetic service provision for haemophilia and other inherited bleeding disorders.
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- 2005
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- Publication type:
- Other
Preimplantation genetic diagnosis: new reproductive options for carriers of haemophilia.
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- Haemophilia, 2004, v. 10, p. 126, doi. 10.1111/j.1365-2516.2004.01042.x
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- Article
Informativeness of linkage analysis for genetic diagnosis of haemophilia A in India.
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- Haemophilia, 2004, v. 10, n. 5, p. 553, doi. 10.1111/j.1365-2516.2004.00908.x
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- Article
Mutation analysis is an essential strategy in the genetic counselling of sporadic haemophilia B families.
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- Haemophilia, 2002, v. 8, n. 5, p. 730, doi. 10.1046/j.1365-2516.2002.00657_2.x
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- Article
Ethical issues in the genetic aspects of haemophilia.
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- Haemophilia, 2002, v. 8, n. 3, p. 268, doi. 10.1046/j.1365-2516.2002.00605.x
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- Article
Counselling about diagnosis and inheritance of genetic bleeding disorders: haemophilia A and B.
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- Haemophilia, 1999, v. 5, n. 2, p. 77, doi. 10.1046/j.1365-2516.1999.00288.x
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- Publication type:
- Article
Genetic service available for counselling and prenatal diagnosis of haemophilia.
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- Haemophilia, 1998, v. 4, p. 24, doi. 10.1046/j.1365-2516.1998.0040s2024.x
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- Publication type:
- Article
Identification and Genetic Analysis of a Factor IX Gene Intron 3 Mutation in a Hemophilia B Pedigree in China.
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- Turkish Journal of Hematology, 2014, v. 31, n. 3, p. 226, doi. 10.4274/tjh.2013.0275
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- Article
Experience of Preimplantation Genetic Diagnosis for Hemophilia at the University Hospital Virgen Del Rocío in Spain: Technical and Clinical Overview.
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- 2015
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- Publication type:
- journal article
Exploring Female Relatives of Patients with Hemophilia' Awareness, Attitudes, and Understanding Towards Genetic Testing.
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- Journal of Multidisciplinary Healthcare, 2024, v. 17, p. 711, doi. 10.2147/JMDH.S430984
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- Publication type:
- Article
Genetic analysis in a female manifesting haemophilia B.
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- 1994
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- Publication type:
- journal article
Genetic Risk Factors for Inhibitor Development in Hemophilia A.
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- Russian Journal of Genetics, 2021, v. 57, n. 8, p. 867, doi. 10.1134/S1022795421080111
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- Article
Genetic Inversions among Hemophilia A Patients from Macedonia and Bulgaria.
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- Acta Haematologica, 2009, v. 120, n. 3, p. 192, doi. 10.1159/000187648
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- Article
Preventing lives affected by hemophilia: A mixed methods study of the views of adults with hemophilia and their families toward genetic screening.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 5, p. N.PAG, doi. 10.1002/mgg3.618
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- Article
Risk stratification integrating genetic data for factor VIII inhibitor development in patients with severe hemophilia A.
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- PLoS ONE, 2019, v. 14, n. 6, p. 1, doi. 10.1371/journal.pone.0218258
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- Article
Understanding of Genetic Inheritance among Xhosa-Speaking Caretakers of Children with Hemophilia.
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- Journal of Genetic Counseling, 2012, v. 21, n. 5, p. 726, doi. 10.1007/s10897-012-9495-9
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- Article
Genetic-Epidemiologic Study of Haemophilia A and B in Hungary.
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- Human Heredity, 1990, v. 40, n. 1, p. 29, doi. 10.1159/000153898
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- Article
Genetic Aspects of Hemophilias A and B in Rio Grande do Sul, Brazil.
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- Human Heredity, 1971, v. 21, n. 2, p. 97, doi. 10.1159/000152390
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- Article
Genetics and Epigenetics in Acquired Hemophilia A: From Bench to Bedside.
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- Current Issues in Molecular Biology, 2024, v. 46, n. 6, p. 5147, doi. 10.3390/cimb46060309
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- Publication type:
- Article
In Vitro Conditioning of Adipose-Derived Mesenchymal Stem Cells by the Endothelial Microenvironment: Modeling Cell Responsiveness towards Non-Genetic Correction of Haemophilia A.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 13, p. 7282, doi. 10.3390/ijms23137282
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- Publication type:
- Article
Mutational analysis of hemophilia B in Russia: Molecular-genetic study.
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- Russian Journal of Genetics, 2016, v. 52, n. 4, p. 409, doi. 10.1134/S1022795416040116
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- Article
Inflammatory and immune response genes: A genetic analysis of inhibitor development in Iranian hemophilia A patients.
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- Pediatric Hematology & Oncology, 2019, v. 36, n. 1, p. 28, doi. 10.1080/08880018.2019.1585503
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- Article
The Clinical Genetics of Hemophilia B (Factor IX Deficiency).
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- Application of Clinical Genetics, 2021, v. 14, p. 445, doi. 10.2147/TACG.S288256
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- Article
Genetic analysis for carrier diagnosis in hemophilia A and B in the Mexican population: 25 years of experience.
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- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 4, p. 939, doi. 10.1002/ajmg.c.31854
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- Article
Robust preimplantation genetic testing of the common F8 Inv22 pathogenic variant of severe hemophilia A using a highly polymorphic multi-marker panel encompassing the paracentric inversion.
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- Thrombosis Journal, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12959-023-00552-w
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- Article