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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 3
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Short Communication

Hb H Hydrops Fetalis Syndrome Caused by Association of the − −SEA Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family

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Pages 216-219 | Received 29 Jul 2014, Accepted 15 Oct 2014, Published online: 21 Apr 2015

References

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  • Charoenkwan P, Sirichotiyakul S, Chanpraph P, et al. Anemia and hydrops in a fetus with homozygous Hemoglobin Constant Spring. J Pediatr Hematol Oncol. 2006;28(12):827–830
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  • Law LW, Lau TK, Fung TY, et al. De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency. BJOG. 2009;116(2):339–343

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