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Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 2
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Original Article

Neonatal Cyanosis Due to A New Gγ-Globin Variant Causing Low Oxygen Affinity: Hb F-Sarajevo [Gγ102(G4)Asn→Thr, AAC>ACC]

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Pages 109-113 | Received 04 Oct 2011, Accepted 09 Nov 2011, Published online: 02 Mar 2012

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (2)

Elisabeth Saller, Elisabeth Kohne, Fabrizio Dutly & Hannes Frischknecht. (2014) A New Gγ-Globin Variant Causing Low Oxygen Affinity: Hb F-Brugine/Feldkirch [Gγ105(G7)Leu→His; HBG2: c.317T>A]. Hemoglobin 38:2, pages 84-87.
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Ho-Wan Ip & Chi-Chiu So. (2013) Diagnosis and prevention of thalassemia. Critical Reviews in Clinical Laboratory Sciences 50:6, pages 125-141.
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Articles from other publishers (9)

Alix Millet, Stéphane Moutereau, Pascal Boileau, Frédéric Galacteros & Emmanuelle Motte‐Signoret. (2022) Neonatal cyanosis with Hb St Mandé, a low O 2 affinity hemoglobin variant affecting β‐globin . Pediatric Blood & Cancer 69:7.
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Vanessa C. Denny, Melinda Fritz, Michael Pollaro & Naureen Memon. (2021) A Failed CCHD Screen. NeoReviews 22:12, pages e840-e842.
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Mark A. Milanick. (2021) Kinesthetic and visual scaffolding for understanding oxygen delivery and reading hemoglobin oxygen curves. Advances in Physiology Education 45:1, pages 121-128.
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Lakshmi Madhumathi Marimuthu & C. G. Delhi Kumar. (2018) Beth-Israel Hemoglobin: An Uncommon Cause of Cyanosis in a 9-year-old Boy. The Indian Journal of Pediatrics 85:9, pages 806-807.
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Jana Lozar-Krivec, Maja Stepic, Tinka Hovnik, Mladen Krsnik & Darja Paro-Panjan. (2016) Neonatal Cyanosis Due to Hemoglobin Variant: Hb F-Sarajevo. Journal of Pediatric Hematology/Oncology 38:7, pages e267-e270.
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Berndt Zur. (2016) Hemoglobin variants – pathomechanism, symptoms and diagnosis. LaboratoriumsMedizin 39:s1.
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Berndt Zur. (2015) Hämoglobinvarianten – Pathomechanismus, Symptome und Diagnostik. LaboratoriumsMedizin 39:5, pages 311-324.
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Monica Pirastru, Paolo Mereu, Sandro Trova, Laura Manca & Bruno Masala. (2014) A new unstable variant of the fetal hemoglobin HBG2 gene: Hb F-Turritana [ G γ64(E8)Gly→Asp, HBG2:c.194G>A] found in cis to the Hb F-Sardinia gene [ A γ(E19)Ile→Thr, HBG1:c.227T>C] . European Journal of Haematology 92:6, pages 510-513.
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P. C. Giordano. (2013) Strategies for basic laboratory diagnostics of the hemoglobinopathies in multi-ethnic societies: interpretation of results and pitfalls. International Journal of Laboratory Hematology 35:5, pages 465-479.
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