The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease
- PMID: 8839734
- DOI: 10.1007/BF01957162
The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease
Comment on
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Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study.Eur J Pediatr. 1995 Nov;154(11):878-81. doi: 10.1007/BF01957496. Eur J Pediatr. 1995. PMID: 8582397
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