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Items: 2

1.

Clinical variability of Waardenburg-Shah syndrome in patients with proximal 13q deletion syndrome including the endothelin-B receptor locus.

Tüysüz B, Collin A, Arapoğlu M, Suyugül N.

Am J Med Genet A. 2009 Oct;149A(10):2290-5. doi: 10.1002/ajmg.a.33031.

PMID:
19764031
2.

Neocentromere at 13q32 in one of two stable markers derived from a 13q21 break.

Rivera H, Vasquez AI, García-Cruz D, Crolla JA.

Am J Med Genet. 1999 Aug 6;85(4):385-8.

PMID:
10398265

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