Browse By Publication: Clinical Genetics
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McInerney-Leo, A.M., Duncan, E.L., Leo, P.J., Gardiner, B., Bradbury, L.A., Harris, J.E., et al. (2015) COL1A1 C-propeptide cleavage site mutation causes high bone mass, bone fragility and jaw lesions: A new cause of gnathodiaphyseal dysplasia? Clinical Genetics, 88(1), pp. 49-55.
Sharman, Rachael R., Sullivan, Karen A., Young, Ross McD., & McGill, Jim (2009) Biochemical markers associated with executive function in adolescents with early and continuously treated Phenylketonuria (ECT-PKU). Clinical Genetics, 75(2), pp. 169-174.
Zee, R. Y., Scbrader, A. P., Robinson, B. G., Griffiths, Lyn R., & Morris, B. J. (1995) Association of HincII RFLP of low density lipoprotein receptor gene with obesity in essential hypertensives. Clinical Genetics, 47(3), pp. 118-121.