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Hemoglobin
international journal for hemoglobin research
Volume 16, 1992 - Issue 5
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Original Article

A Second Observation of the Fetal Methehoglobin Variant HB F-M-Fort Ripley or α2Gγ292(F8)HIS→TYR

T. P. Molchanova Laboratory of Protein Chemistry and Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
J. B. Wilson Laboratory of Protein Chemistry and Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
L-H. Gu Laboratory of Protein Chemistry and Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
R. D. W. Hain Haematology Diagnostic Laboratory The Hospital for Sick Children, Toronto, Ontario, M5G 1X8, Canada
,
L. S. Chang Haematology Diagnostic Laboratory The Hospital for Sick Children, Toronto, Ontario, M5G 1X8, Canada
,
A. O. Poon Haematology Diagnostic Laboratory The Hospital for Sick Children, Toronto, Ontario, M5G 1X8, Canada
&
T. H. J. Huisman Laboratory of Protein Chemistry and Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
 show all
Pages 389-398 | Received 26 Feb 1992, Accepted 03 Jun 1992, Published online: 07 Jul 2009

Citations (18)

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Erin Dainer, Richard Shell, Randy Miller, Joan F. Atkin, Matt Pastore, Abdullah Kutlar, Lina Zhuang, Leslie Holley, Debra H. Davis & Ferdane Kutlar. (2008) Neonatal Cyanosis Due to a Novel Fetal Hemoglobin: Hb F-Circleville [Gγ63(E7)His→Leu, CAT>CTT]. Hemoglobin 32:6, pages 596-600.
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Claude Préhu, Mohamed Rhabbour, Jean Claude Netter, Mathias Denier, Jean Riou, Frédéric Galactéros & Henri Wajcman. (2003) Hb F‐M‐Osaka [Gγ63(E7)His→Tyr] in a Newborn from Southwest France. Hemoglobin 27:1, pages 27-30.
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D. D. Pobedimskaya, T. P. Molchanova, T. H. J. Huisman, S. R. Harding & R. Bakanec. (1993) HB F-Saskatoon or α2Gγ221(B3)GLU→LYS Observed in a North American Indian Newborn. Hemoglobin 17:6, pages 547-549.
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T. P. Molchanova, Yu. V. Postnikov, J. J. Wilson, B. B. Webber, L-H. Gu, H. Sabio, P. Waldron & T. H. J. Huisman. (1993) HB Madrid or α2β2115(G17)ALA→PRO in a Black Teenager. Hemoglobin 17:3, pages 251-254.
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T. P. Molchanova, Yu. V. Postnikov, J. F. Prior, J. L. Raven & J. A. Bennett. (1993) HB Tigraye OR α2β279(EF3)ASP→HIS(GAC→CAC): A Hemoglobin Variant with Increased Oxygen Affinity Observed in an Ethiopian Male. Hemoglobin 17:3, pages 247-250.
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Articles from other publishers (13)

Allison N. J. Lyle, Rebecca Spurr, Danielle Kirkey, Catherine M. Albert, Zeenia Billimoria, Jose Perez & Mihai Puia-Dumitrescu. (2022) Case report of congenital methemoglobinemia: an uncommon cause of neonatal cyanosis. Maternal Health, Neonatology and Perinatology 8:1.
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Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 261 324 .
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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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.
Crossref
Pedro A. de Alarcón & Karen S. Fernández. 2013. Neonatal Hematology. Neonatal Hematology 172 208 .
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.
Crossref
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.
Crossref
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.
Crossref
Laura Manca & Bruno Masala. (2008) Disorders of the synthesis of human fetal hemoglobin. IUBMB Life 60:2, pages 94-111.
Crossref
R. Hojas, A. Villegas, P. Ropero, F. Valverde, A. Nogales, F. A. González, C. José, L. Villar & C. García. (2003) Two new mutations in cis on Gγ chain of fetal hemoglobin: Hb F-Madrid [Gγ50(D1)Ser→Cys] and [Gγ75(E19)Ile→Thr]. Annals of Hematology 82:3, pages 181-183.
Crossref
T.H.J. Huisman. (1997) Gamma chain abnormal human fetal hemoglobin variants. American Journal of Hematology 55:3, pages 159-163.
Crossref
Richard D. W. Hain, David Chitayat, Robert Cooper, Elizabeth Bandler, Barry Eng, David H. K. Chui, John S. Waye & Melvin H. Freedman. (1994) Hb FM-Fort Ripley: Confirmation of autosormal dominant inheritance and diagnosis by PCR and direct nucleotide sequencing. Human Mutation 3:3, pages 239-242.
Crossref

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