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Wiley, American Journal of Medical Genetics, 4(99), p. 308-313, 2001

DOI: 10.1002/ajmg.1181

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Refined FISH characterization of a de novo 1p22-p36.2 paracentric inversion and associated 1p21-22 deletion in a patient with signs of 1p36 microdeletion syndrome

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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