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Chromosome 10p deletion in a patient with hypoparathyroidism, severe mental retardation, autism and basal ganglia calcifications

✍ Scribed by Annapia Verri; Paola Maraschio; Koen Devriendt; Carla Uggetti; Emanuela Spadoni; Edward Haeusler; Antonio Federico

Book ID: 113455307
Publisher: Elsevier Science
Year: 2004
Tongue: English
Weight: 184 KB
Volume: 47
Category: Article
ISSN: 0003-3995
DOI: 10.1016/j.anngen.2004.03.001

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