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Wiley, American Journal of Medical Genetics, 3(122A), p. 261-265, 2003

DOI: 10.1002/ajmg.a.20287

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Narrowing the candidate region of Albright hereditary osteodystrophy-like syndrome by deletion mapping in a patient with an unbalanced cryptic translocation t(2;6)(q37.3;q26)

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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