Delta-Thalassemia

A hereditary disorder characterized by reduced or absent DELTA-GLOBIN thus effecting the level of hemoglobin a2, a minor component of adult hemoglobin monitored in the diagnosis of beta-thalassemia.


Images

the crystal structure of a binary u5 snrnp complex

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(the currently featured pic at MCB) for an example of a picture generated using PDB data. I wouldn't rush things though, or get too strident about immediate deletion. It is clear the images are replaceable. I suggest getting WP:MCB on board to help find all such images that were obtained from the PDB, to tag them as replaceable and make a list, and then generate replacements and replace them. Pushing for immediate deletion may alienate people prepared to do work on this. Carcharoth (talk) 00:36, 20 February 2008 (UTC)

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Diagnosis and therapies

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Symptoms and diagnosis

Symptoms:

    

Wikipedia

Hemoglobin Constant Spring - Wikipedia

More information

Reported cases - Summary of cases reported on this diseaseWHO - World Health OrganizationPubMed - A service of the National Library of Medicine and National Institutes of HealthMEDLINE - Literature from the National Library of MedicineMeSH - Medical Subject HeadingsDeCS - Health Sciences Descriptors
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