Published in Am J Hum Genet on December 01, 1957
Genetic control of some serum proteins in normal humans. Nature (1955) 6.63
A possible case of delayed mutation in man. Ann Hum Genet (1956) 3.84
The blood groups in peptic ulceration. Br Med J (1956) 3.41
The familial incidence of low pseudocholinesterase level. Lancet (1956) 3.24
Blood groups in diabetes mellitus. Br Med J (1956) 3.11
Hereditary deaf mutism, with particular reference to Northern Ireland. Ann Hum Genet (1956) 2.99
Heredofamilial juvenile muscular atrophy simulating muscular dystrophy. AMA Arch Neurol Psychiatry (1956) 2.91
Heredity in gout and hyperuricemia. Acta Med Scand (1955) 2.58
The blood groups of the Hottentots. Am J Phys Anthropol (1955) 2.54
Paget's disease of bone; incidence and subclinical forms. Lancet (1956) 2.37
The ABO blood groups and the sex ratio. Hum Biol (1956) 2.24
The sickle-cell and haemoglobin C genes in some African populations. Ann Hum Genet (1956) 2.12
Telangiectasis of the retina and Coats' disease. Am J Ophthalmol (1956) 2.12
The genetically significant radiation dose from the diagnostic use of x-rays in England and Wales; a preliminary survey. Lancet (1956) 1.92
Hereditary forms of rickets and osteomalacia. J Bone Joint Surg Br (1956) 1.92
[Family incidence of idiopathic torsion dystonia]. Nervenarzt (1956) 1.85
Fertility and blood groups of some East Anglian blood donors. Ann Hum Genet (1956) 1.76
Maintenance of high sickling rate in an African community. Br Med J (1956) 1.75
Serum protein concentrations in the North American Negroid. Science (1956) 1.71
Nail-patella syndrome: clinical and linkage data on family G. Ann Hum Genet (1956) 1.69
Hemoglobin J. Science (1956) 1.69
Sickle-cell anaemia and haemoglobin C. Trans R Soc Trop Med Hyg (1956) 1.67
Two more families with cardiomegaly. Br Heart J (1956) 1.66
A new coagulation defect. Br J Haematol (1956) 1.65
Infantile genetic agranulocytosis; agranulocytosis infantilis hereditaria. Acta Paediatr Suppl (1956) 1.59
Natural selection associated with the ABO blood group. Science (1956) 1.56
Carcinoma of stomach in relation to ABO blood-groups. Lancet (1956) 1.55
The neuropsychiatric aspects of familial dysautonomia (the Riley-Day syndrome). J Ment Sci (1956) 1.55
The genetics of human haemoglobin differences: problems and perspectives. Ann Hum Genet (1956) 1.53
Chronic splenomegaly. Indian J Med Res (1956) 1.53
[Selection by means of incompatibility in the ABO blood group system between mother and fetus; contribution to selection and compensation processes]. Blut (1956) 1.50
Sporadic non-endemic goitrous cretinism; hereditary transmission. Lancet (1956) 1.48
Observations on inheritance and heterogeneity of chronic spherocytosis. Trans Assoc Am Physicians (1955) 1.45
Mortality in relation to histologic type in Hodgkin's disease. Blood (1956) 1.43
Chromosomes in cancer tissue. Ann N Y Acad Sci (1956) 1.30
Sickling and malaria in the Gold Coast. Br Med J (1956) 1.25
The Diego blood factor in Chinese and Japanese. Nature (1956) 1.21
Hereditary hematuria, nephropathy and deafness; preliminary report. N Engl J Med (1956) 1.18
Familial cardiomegaly. Br Heart J (1956) 1.17
Four cases of benign left bundle branch block in the same family. Am Heart J (1956) 1.14
Familial agamma-globulinaemia. Br Med J (1956) 1.14
Acute and latent porphyria. Lancet (1956) 1.13
Heritable disorders of connective tissue. V. Osteogenesis imperfecta. J Chronic Dis (1956) 1.12
Demonstration of the phenotype Le (a+ B+) in infants and in adults. Br J Haematol (1956) 1.11
Further observations on ABO blood-group frequencies and toxaemia of pregnancy. Br Med J (1956) 1.10
[Not Available]. Acta Paediatr Suppl (1956) 1.07
The accuracy of estimates of MNS gene frequences. Acta Genet Med Gemellol (Roma) (1956) 1.07
Production of O inagglutinability in erythrocytes coated with typhoid Vi and O antigens. Nature (1955) 1.06
Familial tuberous sclerosis. Br Med J (1956) 1.05
The calculation of morbid risk in parents of index cases, as applied to a family sample of schizophrenics. Acta Genet Stat Med (1955) 1.05
The production of tears in familial dysautonomia; preliminary report. J Pediatr (1956) 1.04
[Familial syndrome of nephropathy with deafness]. J Urol Medicale Chir (1956) 1.04
A further example of haemoglobin D in a Turkish family. Trans R Soc Trop Med Hyg (1956) 1.03
High incidence blood group found in Venezuelan Indians. Science (1956) 1.02
Color vision in native races in Australasia. Am J Ophthalmol (1956) 1.01
Heritable disorders of connective tissue. VII. The Hurler syndrome. J Chronic Dis (1956) 1.01
Hereditary transient muscular paralysis in Denmark; genetic aspects of family periodic paralysis and family periodic adynamia. Acta Genet Stat Med (1955) 1.00
Sickling in relation to morbidity from malaria and other diseases. Br Med J (1956) 1.00
[Pathogenesis of nevus cells and genetic relationship between nevus pigmentosus, blue nevus, and Recklinghausen's phakomatosis]. Hautarzt (1956) 1.00
Hereditary cerebellar ataxia; olivopontocerebellar type. Neurology (1956) 0.99
Chronic idiopathic jaundice; two cases occurring in siblings, with histochemical studies. Am J Med (1956) 0.99
Cranial manifestations of familial metaphyseal dysplasia. Radiology (1956) 0.99
Intelligence and family size. Psychol Bull (1956) 0.99
Solitary polyps of the colon and rectum: a study of inherited tendency. Am Surg (1956) 0.98
Familial peroneal muscular atrophy and its association with the familial ataxias and tremor and longevity. J Neurol Neurosurg Psychiatry (1956) 0.98
[Association of so-called R. Hunt's dyssynergia cerebellaris myoclonica with Friedreich's spinocerebellar hereditary degeneration; clinical and electromyographic investigations in a case]. Rev Neurol (Paris) (1955) 0.98
Genetic aspects of preadolescent schizophrenia. Am J Psychiatry (1956) 0.97
Congenital atresia of the esophagus in brothers. J Thorac Surg (1956) 0.96
The production of the human blood group A and B genes in individuals belonging to group AB. Nature (1956) 0.96
[Examination of twins for determination of heredity of some anthropologic measures and constitutional indices]. Z Mensch Vererb Konstitutionsl (1956) 0.95
Congenital familial deficiency of factor V (parahaemophilia) combined with deficiency of antihaemophilic globulin. Br J Haematol (1956) 0.94
Thalassemia in Sikhs. Blood (1956) 0.93
Data on linkage in man: hereditary deafness in Northern Ireland. Ann Hum Genet (1956) 0.92
Studies on hemoglobin E. II. The incidence of hemoglobin E in Thailand. J Lab Clin Med (1956) 0.92
Blood groups and disease: rheumatic fever. Australas Ann Med (1956) 0.91
Homozygous hemoglobin C disease in siblings: further comment on intraerythrocytic crystals. Blood (1956) 0.89
[Not Available]. Ophthalmologica (1956) 0.88
Haemoglobin E in Burmese; two cases of haemoglobin E disease. Br Med J (1956) 0.88
[Not Available]. Doc Ophthalmol Proc Ser (1955) 0.88
[Familial polymorphous photo-exanthema]. Arch Klin Exp Dermatol (1956) 0.88
Diabetes insipidus; clinical and experimental studies with consideration of genetic relationships. AMA Arch Intern Med (1955) 0.87
Heritable disorders of connective tissue. VI. Pseudoxanthoma elasticum. J Chronic Dis (1956) 0.87
[A brother and sister with familial infantile diffuse sclerosis of the Krabbe type]. Zentralbl Allg Pathol (1956) 0.87
Congenital atresia of the ileum in two brothers; case report. J Pediatr (1956) 0.87
[Genetic bases of sexual constitution in humans]. Z Mensch Vererb Konstitutionsl (1956) 0.87
Observations on the hereditary nature of Hageman trait. Blood (1956) 0.86
A hitherto undescribed human blood group Am. Br J Haematol (1956) 0.86
Three cases of microlithiasis alveolaris pulmonum occurring in one family. Sci Rep Res Inst Tohoku Univ Med (1955) 0.86
Haemoglobin D in Indians of Gujerati origin in Uganda. East Afr Med J (1956) 0.85
Sex-linked hereditary nystagmus. Pediatrics (1956) 0.85
A blood group genetical survey in Cook Islanders, Polynesia, and comparisons with American Indians. Am J Phys Anthropol (1955) 0.85
The molecular concept of hereditary diseases. Bull Tufts N Engl Med Cent (1956) 0.84
Distribution of the S and C haemoglobin variants in two Nigerian communities. Trans R Soc Trop Med Hyg (1956) 0.83
Hereditary hemorrhagic telangiectasia; report of a case with hemothorax. J Thorac Surg (1956) 0.83
The abnormal hemoglobins. J Natl Med Assoc (1956) 0.83
Variation in homozygous cystinuria. Acta Genet Stat Med (1955) 0.83
A contribution to the heredity of the P.T.C. taste character based on a study of 845 sib-pairs. Ann Hum Genet (1956) 0.83
Glucose-tolerance test: a comparison of results in the African and European. S Afr J Lab Clin Med (1955) 0.83
Abnormal haemoglobins in the Kasai province of the Belgian Congo. Nature (1956) 0.82
Dentinogenesis imperfecta in a racial isolate with multiple hereditary defects. Oral Surg Oral Med Oral Pathol (1956) 0.82
Population differences in red and green color vision deficiency: a review, and a query on selection relaxation. Eugen Q (1962) 1.65
Population differences in vision acuity: a review, with speculative notes on selection relaxation. Eugen Q (1962) 1.32
Early menarchial age of diabetic women. Diabetes (1962) 1.15
An approach to the question, does all diabetes depend upon a single genetic locus? Diabetes (1962) 1.10
Tentative explanation of the high incidence of diabetes. Diabetes (1958) 1.08
Modern therapy and hereditary diseases. Acta Genet Stat Med (1957) 1.04
Transitory "positive" selection for colorblindness? Eugen Q (1963) 0.76
Bibliography of human genetics. Am J Hum Genet (1959) 0.75
Bibliography of human genetics. Am J Hum Genet (1958) 0.75
Bibliography of human genetics. Am J Hum Genet (1958) 0.75
LATERAL LIGAMENT ANKLE SPRAINS. A CLINICAL-PATHOLOGICAL CORRELATION BASED ON THE PRODUCTION AND EXAMINATION OF CONTROLLED SPRAINS IN PREAMPUTATED EXTREMITIES. J Trauma (1964) 0.75
APPRAISALS OF CIVILIZED MAN AND SAVAGE. Eugen Q (1964) 0.75
EUGENICS AND THE I.U.C.D.'S. Eugen Q (1965) 0.75
SELECTION AGAINST "COLORBLINDNESS" AMONG "PRIMITIVE" POPULATIONS. Eugen Q (1965) 0.75
HEARING ACUITY VARIATION AMONG NEGROES AND WHITES. Eugen Q (1964) 0.75
"COLORBLINDNESS" AND RELAXED SELECTION. Eugen Q (1963) 0.75