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107564
[New chromosomal syndromes].

Rev Pediatr Obstet Ginecol Pediatr, 1978/10-1978/12;27(4):343-62.

Duca D, Meilă P, Ursuleanu I, Maximillian C

PMID: 107564

MeSH terms
Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Humans; Phenotype; Translocation, Genetic
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