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Hemoglobin
international journal for hemoglobin research
Volume 25, 2001 - Issue 4
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Hb LIMASSOL [β8(A5)Lys → Asn]: A NEW HEMOGLOBIN VARIANT

Antroulla Kyrri Thalassemia Center, Archbishop Makarios III Hospital, Nicosia, 1474, Cyprus
,
Xenia Felekis Thalassaemia Molecular Genetics Department, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, Nicosia, 1683, Cyprus
,
Eleni Kalogerou Thalassemia Center, Archbishop Makarios III Hospital, Nicosia, 1474, Cyprus
,
George Christopoulos Thalassaemia Molecular Genetics Department, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, Nicosia, 1683, Cyprus
,
Christiana Makariou Thalassemia Center, Archbishop Makarios III Hospital, Nicosia, 1474, Cyprus
,
Dena Loizidou Thalassemia Center, Archbishop Makarios III Hospital, Nicosia, 1474, Cyprus
&
Marina Kleanthous Thalassaemia Molecular Genetics Department, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, Nicosia, 1683, Cyprus
 show all
Pages 421-424 | Received 15 Jun 2001, Accepted 16 Jul 2001, Published online: 07 Jul 2009

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Kazi N. Hasan, Abu Sufian, Ashish K. Mazumder, M. Abdul Khaleque, Mizanur Rahman & Sharif Akhteruzzaman. (2019) A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (HBB: c.27delG) in a Bangladeshi Family Acquired De Novo. Hemoglobin 43:3, pages 162-165.
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Satyabrata Meher, Snehadhini Dehury, Arpita Jana, Subhra Bhattacharya, Amrita Patel, Kishalaya Das, Siris Patel, Biswanath Sarkar & Pradeep Kumar Mohanty. (2016) First Report of Hb Limassol [β8(A5)Lys→Asn; HBB: c.27G>C] from Odisha, India. Hemoglobin 40:6, pages 422-424.
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Andreani R. Kyrri, Xenia Felekis, Eleni Kalogerou, Barbara J. Wild, Loukas Kythreotis, Marios Phylactides & Marina Kleanthous. (2009) Hemoglobin Variants in Cyprus. Hemoglobin 33:2, pages 81-94.
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Articles from other publishers (2)

Jeanne M. Rhea & Ross Molinaro. (2014) Pathology Consultation on HbA1c Methods and Interferences. American Journal of Clinical Pathology 141:1, pages 5-16.
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Juan R. Alvarez-Dominguez, Olga Amosova & Jacques R. Fresco. (2013) Self-catalytic DNA Depurination Underlies Human β-Globin Gene Mutations at Codon 6 That Cause Anemias and Thalassemias. Journal of Biological Chemistry 288:16, pages 11581-11589.
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