Published in Am J Hum Genet on July 01, 1972
Equilibrium frequencies in X-linked recessive disease. Am J Hum Genet (1973) 1.31
Determining the frequency of sporadic cases of rare X-linked disorders. Ann Transl Med (2016) 0.75
Public health and long-term genetic implications of intrauterine diagnosis and selective abortion. Birth Defects Orig Artic Ser (1971) 2.28
Variability and heritability of human fertility. Ann Hum Genet (1970) 1.71
Lesch-Nyhan syndrome: preventive control by prenatal diagnosis. Science (1970) 1.31
The association of juvenile diabetes mellitus and optic atrophy: clinical and genetical aspects. Q J Med (1966) 3.00
Public health and long-term genetic implications of intrauterine diagnosis and selective abortion. Birth Defects Orig Artic Ser (1971) 2.28
Family studies on ocular refraction and its components. J Med Genet (1966) 1.87
Population genetic studies in the Congo. I. Glucose-6-phosphate dehydrogenase deficiency, hemoglobin S, and malaria. Am J Hum Genet (1966) 1.72
Population genetic studies in the Congo. 3. Blood groups (ABO, MNSs, Rh, Jsa). Am J Hum Genet (1966) 1.40
Sex-linked recessive congenital deafness and the excess of males in profound childhood deafness. Ann Hum Genet (1965) 1.36
On the familial predisposition to favism. Am J Hum Genet (1966) 1.29
Genetics of protan and deutan color-vision anomalies: an instructive family. Am J Hum Genet (1969) 1.25
The short-term reduction in birth incidence of recessive diseases as a result of genetic counselling after the birth of an affected child. Hum Hered (1972) 1.13
Gene frequencies in a Dutch population. Hum Hered (1974) 1.12
Common variable immunodeficiency, Hodgkin's disease, and other malignancies in a Newfoundland family. Lancet (1975) 1.12
Pathology of the ear in the cardioauditory syndrome of Jervell and Lange-Nielsen (recessive deafness with electrocardiographic abnormalities). J Laryngol Otol (1966) 1.07
Population genetic studies in the Congo. IV. Haptoglobin and transferrin serum groups in the Congo and in other African population.s. Am J Hum Genet (1966) 1.07
The causes of severe visual handicap among schoolchildren in South Australia. Med J Aust (1968) 1.04
The long-term genetical effects of recent advances in the treatment and prevention of inherited disease. Br J Psychiatry (1974) 1.02
Association of juvenile diabetes mellitus, primary optic atrophy and perceptive hearing loss in three sibs, with additional idiopathic diabetes mellitus insipidus in one case. Acta Endocrinol (Copenh) (1970) 1.00
Glucose-6-phosphate dehydrogenase (G6PD) deficiency, abnormal haemoglobins, and thalassaemia in Yugoslavia. J Med Genet (1966) 0.98
Estimation of the recombination fraction between the protan and deutan loci. Am J Hum Genet (1969) 0.98
Genetic influences on serum cholesterol in two Greek villages. Hum Hered (1969) 0.95
Dysplasia spondyloepiphysaria congenita and related generalized skeletal dysplasias among children with severe visual handicaps. Arch Dis Child (1969) 0.95
Gene frequencies at loci determining blood-group and serum-protein polymorphisms in two villages of northwestern Greece. Am J Hum Genet (1969) 0.93
A comparison of the two-generation and three-generation methods of estimating linkage values on the X chromosome in man with special reference to the loci determining the Xg blood group and glucose-6-phosphate dehydrogenase deficiency. Am J Hum Genet (1968) 0.88
The spectrum of causation of profound deafness in childhood. J Otolaryngol Soc Aust (1968) 0.87
Further data from Greece on recombination between the Xg blood group and glucose-6-phosphate dehydrogenase deficiency. Am J Hum Genet (1968) 0.87
Choroideremia in a female. Br Med J (1968) 0.86
Pathology of the ear in the cardio-auditory syndrome of Jervell and Lange-Nielsen. Report of a third case with an appendix on possible linkage with the Rh blood group locus. J Laryngol Otol (1968) 0.86
The implications of prevention and treatment of inherited disease for the genetic future of mankind. J Genet Hum (1972) 0.83
Pendred syndrome: evidence for genetic homogeneity and further refinement of linkage. J Med Genet (1997) 0.82
A search for associations between genetical polymorphic systems and physical, biochemical and Haematological variables. Hum Hered (1974) 0.82
Genetical influences on serum--cholesterol level. Lancet (1971) 0.82
Children of phenylketonuric women. Pediatrics (1968) 0.80
Serum polymorphisms in Yugoslavia. Hum Hered (1969) 0.79
Population genetic studies in the Congo. II. Effect of hemoglobin S and glucose-6-phosphate dehydrogenase deficiency on mortality and fertility. Am J Hum Genet (1966) 0.79
Epidemiology of profound childhood deafness. Audiology (1974) 0.78
The genetics of thyroid disease. Prog Med Genet (1969) 0.77
Karyotype studies among children with severe visual handicap. Br J Ophthalmol (1970) 0.76
The causes of profound deafness in childhood. In: Sensorinerual hearing loss. Ciba Found Symp (1970) 0.76
The role of genetic factors in the causation of human deafness. Audiology (1972) 0.76
Genetical aspects of severe visual impairment in childhood. J Med Genet (1970) 0.75
A kindred with familial cold urticaria: linkage analysis. J Med Genet (1974) 0.75
The linkage between protan and deutan loci. Am J Hum Genet (1970) 0.75
Genetics and medicine. 3. Br Med J (1966) 0.75
A familial aggregate of common variable immunodeficiency, Hodgkin disease and other malignancies in Newfoundland--I. Clinical features. Clin Invest Med (1979) 0.75
Genetics and medicine. II. Br Med J (1966) 0.75
Genetical implications of ante-natal diagnosis. Ann Genet (1973) 0.75
Genetics and medicine. I. Br Med J (1966) 0.75
Genetical load in man. Humangenetik (1974) 0.75
The handless and footless families of Brazil. Lancet (1970) 0.75
Congenital internal carotid--internal jugular fistula. J Pediatr (1971) 0.75
Effects of antenatal diagnosis and selective abortion on frequencies of genetic disorders. Clin Obstet Gynaecol (1980) 0.75
Clonal origin for individual Burkitt tumours. Lancet (1970) 0.75
A familial aggregate of common variable immunodeficiency, Hodgkin disease and other malignancies in Newfoundland--II. Genealogical analysis and conclusions regarding hereditary determinants. Clin Invest Med (1979) 0.75
Genetic approaches to the nosology of deafness. Birth Defects Orig Artic Ser (1971) 0.75
The effects on society of the treatment of hereditary disturbances of metabolism. Pharm Weekbl (1972) 0.75
Superoxide dismutase variants in Newfoundland--a gene from Scandinavia? Hum Hered (1976) 0.75
[Population genetics]. Ned Tijdschr Geneeskd (1975) 0.75
Iminoglycinuria--a "harmless" inborn error of metabolism? Humangenetik (1968) 0.75
The genetics of congenital deafness. Otolaryngol Clin North Am (1971) 0.75
Diabetes as a risk of parents of children with rare recessive disorders. Lancet (1973) 0.75
The Prevention of Consumption. Br Med J (1885) 0.75