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Ann Genet. 1998;41(3):161-3.

Duplication 10q22.1-q25.1 due to intrachromosomal insertion: a second case.

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1
Department of Paediatrics, Gippsland Hospital, Sale, Australie.

Abstract

This is the second reported case of duplication for the segment 10q22.1-q25.1, the first having been in a fetal case. The phenotype is documented in a 12 year old girl, who is mentally retarded and has a distinctive facial dysmorphology.

PMID:
9833071
[Indexed for MEDLINE]
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