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A boy with mild mental retardation, mild sensorineural hearing loss and mild facial dysmorphism caused by a 19p13.2 deletion: A case report and review of the literature

✍ Scribed by Schwemmle, Cornelia; Rost, Imma; Spranger, Stephanie; Jungheim, Michael; Ptok, Martin


Book ID
122108424
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
870 KB
Volume
78
Category
Article
ISSN
0165-5876

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