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The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease

✍ Scribed by K. Devriendt; B. Eyskens; A. Swillen; M. Dumoulin; M. Gewillig; J. -P. Fryns

Book ID: 105413650
Publisher: Springer
Year: 1996
Tongue: English
Weight: 130 KB
Volume: 155
Category: Article
ISSN: 0340-6997
DOI: 10.1007/bf01957162

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