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Hemoglobin
international journal for hemoglobin research
Volume 22, 1998 - Issue 2
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Original Article

Short Communication:HB Taybe: Description of Genetics and Laboratory Findings in an Israeli Arab Family

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Pages 161-166 | Received 17 Nov 1997, Accepted 20 Jan 1998, Published online: 07 Jul 2009

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Read on this site (3)

Maja Bech Juul, Hanne Vestergaard, Jesper Petersen & Henrik Frederiksen. (2012) Thrombosis in Hb Taybe [codons 38/39 (–ACC) (α1)]. Hemoglobin 36:6, pages 600-604.
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Maria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, Susanna Barella, Maria Franca Desogus & Renzo Galanello. (2012) First Detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in An Italian Child. Hemoglobin 36:3, pages 299-304.
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Varvara Douna, Dimitra Liapi, Dimitrios Kampourakis, Zoe Repapinou, Ioannis Papassotiriou, Alexandra Stamoulakatou, Christos Poziopoulos, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2008) First Observation of Hb Taybe [Codons 38/39 (−Acc) Thr→0 (α1)] In Greece: Clinical and Hematological Findings in Patients With Co-Inherited α+-Thalassemia Mutations. Hemoglobin 32:4, pages 371-378.
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Articles from other publishers (3)

Ariel Koren, Carina Levin, Luci Zalman, Haya Palmor, Dvora Filon, Evgeny Chubar, Peretz Resnitzky & Michael Bennett. (2016) Hb TAYBE: clinical and morphological findings IN 43 patients. European Journal of Haematology 97:2, pages 137-144.
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Shmuel Arnon, Hannah Tamary, Orly Dgany, Ita Litmanovitz, Rivka Regev, Sofia Bauer, Tzipora Dolfin, Joanne Yacobovich, Baruch Wolach & Lutfi Jaber. (2004) Hydrops fetalis associated with homozygosity for hemoglobin Taybe (α 38/39 THR deletion) in newborn triplets. American Journal of Hematology 76:3, pages 263-266.
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Varda Oron-Karni, Dvora Filon, Yulia Shifrin, Elchanan Fried, Galina Pogrebijsky, Ariella Oppenheim & Deborah Rund. (2000) Diversity of ?-globin mutations and clinical presentation of ?-thalassemia in Israel. American Journal of Hematology 65:3, pages 196-203.
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