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Merck
CN
  • A new mutation causing inherited growth hormone deficiency: a compound heterozygote of a 6.7 kb deletion and a two base deletion in the third exon of the GH-1 gene.

A new mutation causing inherited growth hormone deficiency: a compound heterozygote of a 6.7 kb deletion and a two base deletion in the third exon of the GH-1 gene.

Human molecular genetics (1993-07-01)
Y Igarashi, M Ogawa, T Kamijo, N Iwatani, Y Nishi, H Kohno, T Masumura, J Koga