Found: 10
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Two new double mutant alleles of the F7 gene and a literature review on alleles with two mutations in FVII deficiency.
- Published in:
- Haemophilia, 2016, v. 22, n. 4, p. e304, doi. 10.1111/hae.12897
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- Article
A new report of FVII-inhibitor in a patient suffering from severe congenital FVII deficiency.
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- Haemophilia, 2015, v. 21, n. 4, p. e336, doi. 10.1111/hae.12708
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- Article
Identification of two novel missense mutations causing severe factor XIII deficiency.
- Published in:
- Haemophilia, 2015, v. 21, n. 3, p. e253, doi. 10.1111/hae.12663
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- Article
Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.
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- Haemophilia, 2014, v. 20, n. 4, p. 568, doi. 10.1111/hae.12340
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- Article
Genotype and phenotype relationships in 10 Pakistani unrelated patients with inherited factor VII deficiency.
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- Haemophilia, 2013, v. 19, n. 6, p. 893, doi. 10.1111/hae.12186
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- Article
Pattern of bleeding and response to therapy in Glanzmann thrombasthenia.
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- Haemophilia, 2012, v. 18, n. 6, p. e423, doi. 10.1111/hae.12017
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- Article
Glanzmann thrombasthenia in Pakistan: molecular analysis and identification of novel mutations.
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- Clinical Genetics, 2016, v. 89, n. 2, p. 187, doi. 10.1111/cge.12622
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- Article
Acute blood transfusion reactions in a tertiary care hospital in Pakistan ‐ an initiative towards haemovigilance.
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- Transfusion Medicine, 2019, v. 29, n. 4, p. 275, doi. 10.1111/tme.12541
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- Article
Frequency and reasons of donor deferral prior to blood donation process: a single centre experience.
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- Transfusion Medicine, 2017, v. 27, n. 1, p. 10, doi. 10.1111/tme.12368
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- Article
Red cell alloimmunisation in regularly transfused beta thalassemia patients in Pakistan.
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- Transfusion Medicine, 2015, v. 25, n. 2, p. 106, doi. 10.1111/tme.12196
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- Article