Published in Am J Med Genet on May 03, 1996
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Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease. Neurology (2008) 1.55
A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3. Am J Hum Genet (1999) 1.54
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Absence of functional receptors for parathyroid hormone and parathyroid hormone-related peptide in Blomstrand chondrodysplasia. J Clin Invest (1998) 1.52
High incidence of SHOX anomalies in individuals with short stature. J Med Genet (2006) 1.51
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