Familial isolated growth hormone deficiency due to a novel homozygous missense mutation in the growth hormone releasing hormone receptor gene: clinical presentation with hypoglycemia.
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K. Hussain | M. Ozbek | H. Demirbilek | A. Baran | P. Shah | V. Arya | R. T. Baran | M. Sherif | Sophia Tahir | N. Hatipoglu