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).

Source:http://linkedlifedata.com/resource/pubmed/id/12966529

Am. J. Med. Genet. A 2003 Oct 15 122A 3 261-5

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PMID
12966529