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A Swiss (εγδβ)0‐thalassemia patient with a novel 3‐Mb deletion associated with mild mental impairment

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Bibliographic Details
Published in:	American journal of hematology 2013-02, Vol.88 (2), p.158-159
Main Authors:	Von Kanel, Thomas, Röthlisberger, Benno, Schanz, Urs, Dutly, Fabrizio, Huber, Andreas R., Saller, Elisabeth
Format:	Article
Language:	English
Subjects:	Abnormalities, Multiple - etiology Abnormalities, Multiple - physiopathology Craniofacial Abnormalities Delayed Diagnosis Developmental Disabilities - etiology Developmental Disabilities - physiopathology Diseases in Twins DNA, Intergenic - genetics Facies Female Gene Deletion Hematology Hemoglobin E - genetics Hemoglobin E - metabolism Hemoglobins - genetics Hemoglobins - metabolism Humans Infant, Newborn Muscular Atrophy - etiology Muscular Atrophy - physiopathology Premature Birth Severity of Illness Index Switzerland Thalassemia - diagnosis Thalassemia - genetics Thalassemia - physiopathology Twins, Dizygotic
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