Published in Am J Public Health Nations Health on July 01, 1966
A world-wide view of venereal disease. Br J Vener Dis (1972) 2.09
Educating teen-agers about venereal disease. J Sch Health (1967) 1.31
Heterogeneity in genetic control of phenylalanine metabolism in man. Nature (1968) 1.19
Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria. J Pediatr (1988) 1.00
Light modulation with resonant grating-waveguide structures. Opt Lett (1996) 0.94
Autosomal dominant polycystic kidney disease in the fetus. Am J Med Genet (1994) 0.94
Histidinemia discovered by urine screening after renal transplantation. Pediatrics (1970) 0.92
Policy statement concerning DNA banking and molecular genetic diagnosis. Canadian College of Medical Geneticists. Clin Invest Med (1991) 0.90
Chromosomal breakage in normal and fragile X subjects using low folate culture conditions. J Med Genet (1983) 0.89
Fragile X. N Engl J Med (1982) 0.88
Tubulointerstitial nephritis in methylmalonic acidemia. Pediatr Nephrol (1993) 0.84
Folate coenzyme forms in fibroblasts from patients deficient in 5,10-methylenetetrahydrofolate reductase. Biochem Soc Trans (1976) 0.82
Anticonvulsants, folate levels, and pregnancy outcome: a prospective study. Ann Neurol (1987) 0.80
Differences in liver folate enzyme patterns in premature and full term infants. Pediatr Res (1982) 0.76
Awareness of physician's social status within an urban community. J Health Hum Behav (1966) 0.75
The home for the aged--theory and practice. Gerontologist (1966) 0.75
Letter: Development of arthritis in Lowe's syndrome. J Pediatr (1974) 0.75
The banking of DNA for the prevention of genetic disease. Clin Invest Med (1991) 0.75
The glioma cell-derived neurite promoting activity protein is functionally and immunologically related to human protease nexin-I. J Cell Physiol (1987) 0.75
Problems of parents with a baby in a special care unit. Midwife Health Visit Community Nurse (1982) 0.75
Who judges the teachers? Science (1966) 0.75
Homocystinuria (methylenetetrahydrofolate reductase deficiency) and mutation of factor V gene. J Inherit Metab Dis (1998) 0.75