Author:
Wajnrajch Michael P.,Gertner Joseph M.,Harbison Madeleine D.,Chua Streamson C.,Leibel Rudolph L.
Publisher
Springer Science and Business Media LLC
Reference24 articles.
1. Rosenfeld, R.G. et al. Diagnostic controversy: the diagnosis of childhood growth hormone deficiency revisited. J. Clin. Endocrin. Metab. 80, 1532–1540 (1995).
2. Phillips, J.A. & Cogan, J.D. Genetic basis of endocrine disease 6: molecular basis of familial human growth hormone deficiency. J. Clin. Endocrin. Metab. 78, 11–16 (1994).
3. Eicher, E.M. & Beamer, W.G. Inherited ateliotic dwarfism in mice. Characteristics of the mutation, little, on chromosome 6. J. Hered.. 67, 87–91 (1976).
4. Chua, S.C., Hennessey, K., Zeitler, P. & Leibel, R.L. The little (lit) mutation cosegregates with the growth hormone releasing factor receptor on mouse chromosome 6. Mamm. Gen. 4, 555–559 (1993).
5. Godfrey, P., Rahal, J.O., Beamer, W.G., Copeland, N.G., Jenkins, N.A. & Mayo, K.E. GHRH receptor of little mice contains a missense mutation in the extracellular domain that disrupts receptor function. Nature Genet. 4, 227–232 (1993).
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