Compound heterozygosity of Hb Hamilton and de novo mutated HbM Saskatoon

Author:

Brunner-Agten Saskia,Hergersberg Martin,Herklotz Roberto,Hirt Andreas,Huber Andreas R.

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Reference8 articles.

1. Nagel RL (2001) Disorders of hemoglobin function and stability. In: Steinberg MH, Forget BG, Higgs DR, Nagel RL (eds) Disorders of hemoglobin. Cambridge University Press, Great Britain, pp 1155–1194

2. Huismann THJ, Carver MFH, Baysal E (1997) A syllabus of thalassemia mutations. Sickle Cell Anemia Foundation, Augusta

3. Old JM (2007) Screening and genetic diagnosis of haemoglobinopathies. Scand J Clin Lab Invest 67:71–86

4. Manca L, Cocco E, Cossu G, Masala B (1992) Identification of Hb Hamilton or beta 11(A8)Val––Ile gene by the polymerase chain reaction amplification technique. Biochim Biophys Acta 1139:17–19

5. Stamatoyannopoulos G, Nute PE (1982) De novo mutations producing unstable Hbs or Hbs M. II. Direct estimates of minimum nucleotide mutation rates in man. Hum Genet 60:181–188

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