Evaluation of SHOX copy number variations in patients with Mullerian aplasia




SANDBACKA M, HALTTUNEN M, Jokimaa V, AITTOMAKI K, LAIVUORI H

2011

 Orphanet Journal of Rare Diseases

53

6

5

1750-1172

DOIhttps://doi.org/10.1186/1750-1172-6-53




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