Deletion (1)(p32.2–p32.3) detected by array-CGH in a...

Deletion (1)(p32.2–p32.3) detected by array-CGH in a patient with developmental delay/mental retardation, dysmorphic features and low cholesterol: A new microdeletion syndrome?

Milene Mulatinho, Juan Llerena, Trond P. Leren, P. Nagesh Rao, Fabiola Quintero-Rivera
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Volume:
146A
Year:
2008
Language:
english
Pages:
7
DOI:
10.1002/ajmg.a.32454
File:
PDF, 122 KB
english, 2008
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