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American Journal of Medical Genetics|April 1, 1992
Nomenclature guidelines for X-linked mental retardationJ C Mulley, B Kerr, R Stevenson, et al.Human Heredity|January 1, 1982
Polymorphism of human galactose-1-phosphate uridyl transferaseJ C MulleyThe Australian Journal of Experimental Biology and Medical Science|April 1, 1982
Distribution of alpha 1-antitrypsin (PI) subtypes from newbornsJ C MulleyThe Australian Journal of Experimental Biology and Medical Science|August 1, 1980
Distribution of the six alpha 1-antitrypsin (PI) subtypes from a sample of blood donorsJ C MulleyAmerican Journal of Medical Genetics|July 12, 1996
X-linked mental retardation with thin habitus, osteoporosis, and kyphoscoliosis: linkage to Xp21.3-p22.12J F Arena, C Schwartz, L Ouzts, et al.The Australian Journal of Experimental Biology and Medical Science|August 1, 1982
Distribution of six TF C (transferrin) subtypes in cord bloods and blood donorsC Nicholls, J C MulleyThe Australian Journal of Experimental Biology and Medical Science|August 1, 1982
Distribution of the GC (group-specific component) subtypes in cord bloods and blood donorsC Nicholls, J C MulleyEuropean Journal of Human Genetics : EJHG|April 10, 1999
Characterisation and expression of a large, 13.7 kb FMR2 isoformJ Gecz, J C MulleyDie Nahrung|January 1, 1987
Serum free amino acids of healthy males and pregnant women from EthiopiaW H Peters, H LubsHuman Genetics|December 1, 1986
New regional localisations for HAGH and PGP on human chromosome 16J C Mulley, D F CallenPageof 89