Clinical Chemistry Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

Clinical Chemistry 46: 139-a-140-a, 2000;
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an electronic Letter to
the Editor about this paper
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (2)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Krauss, J. S.
Right arrow Articles by Kenimer, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Krauss, J. S.
Right arrow Articles by Kenimer, E.
Related Collections
Right arrow Molecular Diagnostics and Genetics
Right arrow Hematology
(Clinical Chemistry. 2000;46:139-140.)
© 2000 American Association for Clinical Chemistry, Inc.

Letters

Elution of Hemoglobin {alpha}Montgomery2ßS2 Hybrid Tetramers by the Variant Apparatus

Jonathan S. Kraussa,1

a Address correspondence to this author at: BIH-222B, MCG, Pathology, 1120 15th St., Augusta GA 30912-3620. Fax 706-721-7837; e-mail jkrauss@mail.mcg.edu.

Keith Bures1
Elizabeth Kenimer1

1 Department of Pathology, Section of Clinical Pathology, Medical College of Georgia, Augusta, GA 30912


To the Editor:

Hemoglobin (Hb) Montgomery ({alpha}48 Leu->Arg) is an uncommon variant first reported in 1975 (1). We report here a case of the association of homozygous HbS (ß6 Glu->Val) with this variant identified by the late Dr. T.H.J. Huisman in an 8-year-old black girl with a life-long sickling disorder.

We quantified Hb fractions by cation-exchange HPLC with the VariantTM Hemoglobin Testing System Beta-Thalassemia Short Program (Bio-Rad Diagnostics) (2)(3). The complete blood count . . . [Full Text of this Article]


References




The following articles in journals at HighWire Press have cited this article:


Home page
 Clin. Chem.Home page
G. M. Clarke and T. N. Higgins
Laboratory Investigation of Hemoglobinopathies and Thalassemias: Review and Update
Clin. Chem., August 1, 2000; 46(8): 1284 - 1290.
[Abstract] [Full Text] [PDF]


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2000 by the American Association for Clinical Chemistry.