Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus.
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I. Bergadá | H. Domené | M. Ropelato | P. Scaglia | H. Jasper | M. Ballerini | A. Keselman | M. E. Rodríguez | María Soledad Rodríguez Prieto