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Clin Dysmorphol. 2010 Jul;19(3):137-9. doi: 10.1097/MCD.0b013e328338807d.

Two adjacent microdeletions in 8q11.2 cause a phenotype suggestive of the 22q11 deletion syndrome.

Author information

1
Department of Human Genetics, Radboud University, Nijmegen Medical Centre, Nijmegen, The Netherlands.
PMID:
20357662
DOI:
10.1097/MCD.0b013e328338807d
[Indexed for MEDLINE]

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