Microcytosis in a 43-Year-Old Man-Reference-Cited by-同舟云学术

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Microcytosis in a 43-Year-Old Man

Published:2010-10 Issue:10 Volume:41 Page:581-583
ISSN:0007-5027
Container-title:Laboratory Medicine
language:en
Short-container-title:Lab Med

Author:

Ong Menchu G.,Veillon Diana M.,Cotelingam James D.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

Link

http://academic.oup.com/labmed/article-pdf/41/10/581/8321794/labmed41-0581.pdf

Reference6 articles.

1. Hoyer JD Kroft SH Fairbanks VF Case studies. Color Atlas of Hemoglobin Disorders: A Compendium Based on Proficiency Testing. Northfield, IL: College of American Pathologists; 2003

2. Sickle cell?haemoglobin E (HbSE) compound heterozygosity: a clinical and haematological study

3. Aksoy M Lehmann H . The first observation of sickle-cell hemoglobin E disease. Nature. 1957;179:1248–1249.

4. Hemoglobin SE disease—A concise review

5. Moo-Penn W Bechtel K Jue D The presence of hemoglobin S and C Harlem in an individual in the United States. Blood. 1975;46:363–367.

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