Artigo
Revisado por pares
A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome
2004; Springer Science+Business Media; Volume: 116; Issue: 1-2 Linguagem: Inglês
10.1007/s00439-004-1195-6
ISSN1432-1203
AutoresKatrina Prescott, Kathryn Woodfine, Paula Stubbs, Maurice Super, Bronwyn Kerr, Rodger Palmer, Nigel P. Carter, Peter Scambler,
Tópico(s)Chromosomal and Genetic Variations
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