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Hemoglobin
international journal for hemoglobin research
Volume 32, 2008 - Issue 6
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Neonatal Cyanosis Due to a Novel Fetal Hemoglobin: Hb F-Circleville [Gγ63(E7)His→Leu, CAT>CTT]

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Pages 596-600 | Received 09 Apr 2008, Accepted 10 Jul 2008, Published online: 07 Jul 2009

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Read on this site (3)

Toon Schiemsky, Joris Penders & Davy Kieffer. (2016) Failing blood gas measurement due to methemoglobin forming hemoglobin variants: a case report and review of the literature. Acta Clinica Belgica 71:3, pages 167-170.
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Niren Patel, Jason Fixler, Yoram Unguru, Abdullah Kutlar & Ferdane Kutlar. (2015) A New Aγ-Globin Chain Variant: Hb F-Sykesville MD [Aγ113(G15)Val → Ile; HBG1: c.340G>A] Detected in a Caucasian Baby. Hemoglobin 39:1, pages 52-54.
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Ferdane Kutlar, Afshin Ameri, Niren H. Patel, Lina Zhuang, Lee E. Johnson, Michael L. Cheng & Abdullah Kutlar. (2014) Two New γ Chain Variants: Hb F-Augusta GA [Gγ59(E3)Lys → Arg; HBG2: c.179A > G] and Hb F-Port Royal-II [Aγ125(H3)Glu → Ala; HBG1: c.377A > C]. Hemoglobin 38:5, pages 376-380.
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Articles from other publishers (14)

Yanru Chen, Jingwen Lv & Jihong Qian. (2024) Case Report: A case report and literature review of hemoglobin variation associated with neonatal cyanosis. Frontiers in Pediatrics 12.
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Shanu Chandran, Benjamin J. Ross & Manish Kumar. (2022) The journey from blue to pink–a rare cause for self-limiting methemoglobinemia in an Indian baby. Case Reports in Perinatal Medicine 11:1.
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Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 261 324 .
Jing Yuan & Xue-Ping Zhu. (2020) Clinical characteristics on manifestation and gene mutation of a transient neonatal cyanosis: A case report. World Journal of Clinical Cases 8:1, pages 217-221.
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Alejandra Young, Uma Dandekar, Calvin Pan, Avery Sader, Jie J. Zheng, Richard A. Lewis & Debora B. Farber. (2016) GNAI3: Another Candidate Gene to Screen in Persons with Ocular Albinism. PLOS ONE 11:9, pages e0162273.
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Thomas A Hooven, Ellen M Hooper, Sandeep N Wontakal, Richard O Francis, Rakesh Sahni & Margaret T Lee. (2016) Diagnosis of a rare fetal haemoglobinopathy in the age of next-generation sequencing. BMJ Case Reports, pages bcr2016215193.
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Almudena Alonso-Ojembarrena & Simón P. Lubián-López. (2016) Hemoglobin M Disease as a Cause of Cyanosis in a Newborn. Journal of Pediatric Hematology/Oncology 38:3, pages 173-175.
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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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Celeste Bento, Tabita Magalhães Maia, Ines Carvalhais, Filipa Moita, Gabriela Abreu, Luis Relvas, Alexandra Pereira, José Farela Neves & Maria L. Ribeiro. (2013) Transient Neonatal Cyanosis Associated With a New Hb F Variant. Journal of Pediatric Hematology/Oncology 35:2, pages e77-e80.
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A. Charon, E. Henrion, S. Delpire, A. Redondi & C. Lecart. (2011) Cyanose néonatale due à une hémoglobine fœtale M-Osaka. Archives de Pédiatrie 18:10, pages 1107-1109.
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Madeleine Verhovsek, Matthew P.A. Henderson, Gerard Cox, Hong‐yuan Luo, Martin H. Steinberg & David H.K. Chui. (2011) Erratum to: Unexpectedly low pulse oximetry measurements associated with variant hemoglobins: A systematic review. American Journal of Hematology 86:8, pages 722-725.
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Moira A. Crowley, Todd L. Mollan, Osheisa Y. Abdulmalik, Andrew D. Butler, Emily F. Goodwin, Arindam Sarkar, Catherine A. Stolle, Andrew J. Gow, John S. Olson & Mitchell J. Weiss. (2011) A Hemoglobin Variant Associated with Neonatal Cyanosis and Anemia. New England Journal of Medicine 364:19, pages 1837-1843.
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Madeleine Verhovsek, Matthew P.A. Henderson, Gerard Cox, Hong‐yuan Luo, Martin H. Steinberg & David H.K. Chui. (2010) Unexpectedly low pulse oximetry measurements associated with variant hemoglobins: A systematic review. American Journal of Hematology 85:11, pages 882-885.
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