Published in Am J Hum Genet on September 01, 1960
Regional mapping of the phenylalanine hydroxylase gene and the phenylketonuria locus in the human genome. Proc Natl Acad Sci U S A (1985) 2.58
The PKU locus in man is on chromosome 12. Am J Hum Genet (1984) 1.42
Phenylketonuria: a linkage study using phenylalanine tolerance tests. Am J Hum Genet (1960) 1.05
Increased reliability for the determination of the carrier state in phenylketonuria. Am J Hum Genet (1961) 0.85
Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio. J Med Genet (1975) 0.81
Sequential tests for the detection of linkage. Am J Hum Genet (1955) 43.74
Detection by phenylalanine tolerance tests of heterozygous carriers of phenylketonuria. Nature (1956) 2.98
A one-year, controlled study of the effect of low-phenylalanine diet on phenylketonuria. Pediatrics (1958) 2.02
Assay of L-phenylalanine as phenylethylamine after enzymatic decarboxylation; application to isotopic studies. J Biol Chem (1953) 1.65
A case of phenylketonuria with borderline intelligence. AMA J Dis Child (1957) 1.25
Phenylketonuria: the phenylalanine-tyrosine ratio in the detection of the heterozygous carrier. J Ment Defic Res (1958) 1.16
Data for the study of linkage in man; phenylketonuria and the ABO and MN loci. Ann Eugen (1951) 1.16
Phenylketonuria: a linkage study using phenylalanine tolerance tests. Am J Hum Genet (1960) 1.05
Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea. Pediatrics (1954) 5.36
A genetic and statistical study of psoriasis. Am J Hum Genet (1951) 3.69
HEREDITARY PROGRESSIVE ARTHRO-OPHTHALMOPATHY. Mayo Clin Proc (1965) 3.51
A reconsideration of the phenomenon of anticipation in diabetes mellitus. Proc Staff Meet Mayo Clin (1950) 3.09
A study of the genetics of diabetes mellitus. Am J Hum Genet (1952) 3.02
Detection by phenylalanine tolerance tests of heterozygous carriers of phenylketonuria. Nature (1956) 2.98
Sequential test for linkage between cystic fibrosis of the pancreas and the MNS locus. Am J Hum Genet (1956) 2.65
Pedigree of a family with hereditary chronic relapsing pancreatitis. Gastroenterology (1952) 2.41
Abnormalities observed during the first six days of life in 8,716 live-born infants. Pediatrics (1954) 2.31
The inheritance of serum haptoglobin types in American Negroes: evidence for a third allele Hp-2m. Am J Hum Genet (1960) 2.28
Erythroblastosis fetalis. VIII. Studies of serum bilirubin in relation to Kernicterus. N Engl J Med (1952) 2.23
A GENETIC STUDY OF THE ANTIGENS ASSOCIATED WITH THE GM(B) FACTOR OF HUMAN GAMMA GLOBULIN. Am J Hum Genet (1965) 2.07
An analysis of the phenomenon of "anticipation" in diabetes mellitus. Ann Intern Med (1952) 2.05
Linkage studies with cystic fibrosis of the pancreas. Am J Hum Genet (1956) 2.04
A one-year, controlled study of the effect of low-phenylalanine diet on phenylketonuria. Pediatrics (1958) 2.02
The hematocrit of capillary blood. N Engl J Med (1955) 1.76
The genetics of diabetes: a review. Ann N Y Acad Sci (1959) 1.70
Variability in the clinical manifestations of galactosemia. J Pediatr (1961) 1.64
The laboratory detection of heterozygotes. Am J Hum Genet (1957) 1.58
Gamma globulin in the prevention of infectious hepatitis; studies on the use of small doses in family outbreaks. N Engl J Med (1954) 1.56
Frequency of genetic transmission of sporadic retinoblastoma. AMA Arch Ophthalmol (1957) 1.52
Serum bilirubin levels in the newborn infant. J Pediatr (1953) 1.51
STUDIES ON THE GM, INV, HP AND TF SERUM FACTORS OF JAPANESE POPULATIONS AND FAMILIES. Hum Biol (1964) 1.49
Pathogenetic problems in phenylketonuria. Am J Med (1957) 1.46
Methodology in human genetics. J Med Educ (1959) 1.42
Age, sex, serum lipids, and coronary atherosclerosis. J Am Med Assoc (1956) 1.39
Heredity and diabetes. Diabetes (1958) 1.39
Hereditary globulin factors and immune tolerance in man. Science (1963) 1.38
Prolonged obstructive jaundice in infancy. IV. Neonatal hepatitis. AMA Am J Dis Child (1954) 1.38
Prolonged obstructive jaundice in infancy. V. The genetic components in neonatal hepatitis. AMA J Dis Child (1958) 1.37
Family outbreaks of infectious hepatitis; prophylactic use of gamma globulin. N Engl J Med (1953) 1.34
A Gm-like factor present in Negroes and rare or absent in whites: its relation to Gma and Gmx. Am J Hum Genet (1960) 1.32
ACID PHOSPHATASES OF HUMAN RED CELLS: PREDICTED PHENOTYPE CONFORMS TO A GENETIC HYPOTHESIS. Science (1964) 1.30
Heredity, environment, and serum cholesterol; a study of 201 healthy families. Circulation (1958) 1.28
Inhibition of glucuronosyl transferase by progestational agents from serum of pregnant women. Nature (1960) 1.25
A new human gamma globulin factor determined by an allele at the Inv locus. Vox Sang (1962) 1.25
A case of phenylketonuria with borderline intelligence. AMA J Dis Child (1957) 1.25
Serum phenylalanine and tyrosine levels in the newborn infant. N Engl J Med (1962) 1.25
Detection of the heterozygous carriers of phenylketonuria. Lancet (1956) 1.23
On the inheritance of the antigen f of the Rh complex. Am J Hum Genet (1954) 1.22
SCREENING NEWBORN INFANTS FOR PHENYLKETONURIA. JAMA (1964) 1.20
DEPENDENCE OF A GM(B) ANTIGEN ON THE QUATERNARY STRUCTURE OF HUMAN GAMMA GLOBULIN. Science (1964) 1.12
Genetic and population studies of the blood types and serum factors among Indians and Chinese from Malaya. Am J Hum Genet (1961) 1.10
The distribution of the gamma globulin types Gm(a), Gm(x) and Gm-like in South and Southeast Asia and Australia. Am J Hum Genet (1963) 1.10
Report of a second example of the Rh agglutinogen cv, with some comments on its relation to the agglutinogen f. Science (1953) 1.09
Epinephrine metabolism in phenylketonuria. Proc Soc Exp Biol Med (1962) 1.08
Birth weight in infants of diabetic mothers. Ann Hum Genet (1957) 1.08
INHIBITION OF GLUCURONOSYL TRANSFERASE BY STEROID HORMONES. Arch Biochem Biophys (1963) 1.05
Birth weight in cystic fibrosis of the pancreas. Ann Hum Genet (1959) 1.04
The heterozygous carrier in galactosaemia. Nature (1958) 1.04
Evidence for a Gm allele negative for both Gm(a) and Gm(b). Vox Sang (1962) 0.99
Studies on the genetic mechanism of cystic fibrosis of the pancreas. AMA J Dis Child (1959) 0.99
The dietary phenylalanine requirements and tolerances of phenylketonuric patients. AMA J Dis Child (1957) 0.98
Antihemophilic factor deficiency in the female. J Lab Clin Med (1958) 0.97
Studies on hereditary gamma globulin factors: detection of the factor Gm-like in a white family. Vox Sang (1963) 0.97
Genetic studies on hypercholesteremia: frequency in a hospital population and in families of hypercholesteremic index patients. Am Heart J (1953) 0.96
Studies on the Gm factors: comparison of the agglutinators in serum from patients with rheumatoid arthritis and in serum from healthy donors. Arthritis Rheum (1962) 0.95
Observations on the new Rh agglutinin anti-f. Blood (1954) 0.95
Glucose-6-phosphate dehydrogenase deficiency in Taiwan. Am J Hum Genet (1963) 0.94
INHIBITORS OF GLUCURONYL TRANSFERASE IN THE NEWBORN. Ann N Y Acad Sci (1963) 0.94
THE GM AND INV GROUPS OF INDIANS FROM SANTA CATARINA, BRAZIL. Am J Hum Genet (1965) 0.92
Clinical course of hyperbilirubinemia in premature infants. A preliminary report. N Engl J Med (1960) 0.90
Galactosemia: a study of twenty-seven kindreds in North America. Ann Hum Genet (1962) 0.89
Further data on symphalangism. J Hered (1948) 0.89
Coproporphyrin studies in children. I. Urinary coproporphyrin excretion in normal children. Proc Soc Exp Biol Med (1954) 0.89
Experimental studies on blood-spinal fluid barrier for bilirubin. J Lab Clin Med (1959) 0.88
A genetically determined human serum factor detected by its effect on a mating reaction in yeast. Am J Hum Genet (1959) 0.87
THE INFLUENCE OF SERUM BILIRUBIN LEVELS UPON THE ULTIMATE DEVELOPMENT OF LOW BIRTHWEIGHT INFANTS. J Ment Defic Res (1965) 0.87
The genetic mechanism of galactosaemia. Arch Dis Child (1960) 0.86
Homologous serum-hepatitis following the use of fraction IV prepared from postpartum plasma; a report of four cases. Am J Med Sci (1953) 0.86
Effect of heat on the serum Gm-a, Gm-b, Gm-x and Gm-like. Nature (1960) 0.86
STUDIES ON GALACTOSE OXIDATION IN DOWN'S SYNDROME. N Engl J Med (1964) 0.86
Further studies on the inheritance of Hageman trait. J Lab Clin Med (1962) 0.85
The genetic mechanism of idiopathic hyperlipemia. N Engl J Med (1957) 0.85
THE RELATION OF THE S AND F FRAGMENTS AND THE H AND L CHAINS OF GAMMA GLOBULIN TO THE GM GROUPS. Vox Sang (1965) 0.85
Pregnancy in the diabetic mother with nephritis. Lancet (1957) 0.84
BRAIN SEROTONIN IN EXPERIMENTAL TYROSINOSIS. Nature (1964) 0.84
THE PRODUCTION OF ANTI-GM REAGENTS BY RHESUS MONKEYS IMMUNIZED WITH POOLED HUMAN GAMMA GLOBULIN. Vox Sang (1964) 0.84
A controlled study on effect of promethazine hydrochloride and meperidine hydrochloride upon serum billirubin levels in the newborn infant. J Pediatr (1963) 0.83
Development of 5-hydroxytryptophan decarboxylase activity in rat kidney. Nature (1960) 0.82
Inborn errors of carbohydrate metabolism. Diabetes (1961) 0.81
POPULATION, IMMUNOGENETIC, AND BIOCHEMICAL STUDIES ON THE GM(B) FACTORS OF HUMAN GAMMA GLOBULIN. Cold Spring Harb Symp Quant Biol (1964) 0.81
Further studies on the heterozygous carrier in galactosemia. J Lab Clin Med (1960) 0.80
Blood glucose-6-phosphate in heterozygous carriers and patients with liver glycogen disease (Von Gierke's disease). Nature (1961) 0.80
Clinical management of phenylketonuria. Q Bull Northwest Univ Med Sch (1962) 0.80
Medical genetics. N Engl J Med (1960) 0.80
Detection of heterozygous carriers in glycogen storage disease of the liver (von Gierke's disease). Nature (1959) 0.78
An inborn error of lipid metabolism. Pediatrics (1959) 0.78
Studies on mechanism for decreased lipoprotein lipase in cystic fibrosis of the pancrease. J Pediatr (1963) 0.78
Medical genetics. N Engl J Med (1960) 0.78
Viral hepatitis. N Engl J Med (1953) 0.78
Lipoprotein lipase in cystic fibrosis of the pancreas. J Lab Clin Med (1962) 0.78
Familial incidence of primary carcinoma of the jejunum. J Am Med Assoc (1951) 0.78
MECHANISMS FOR THE DECREASE OF BRAIN SEROTONIN. Nature (1963) 0.78
STUDIES ON INHIBITION OF BRAIN 5-HYDROXYTRYPTOPHAN DECARBOXYLASE BY PHENYLALANINE METABOLITES. Proc Soc Exp Biol Med (1965) 0.76
Studies on the heterozygous carrier in galactosemia. J Lab Clin Med (1959) 0.76
[Not Available]. J Genet Hum (1954) 0.76
A further note on the genetics of psoriasis. Am J Hum Genet (1952) 0.75
LINKAGE STUDIES WITH THE HUMAN RED BLOOD CELL ACID PHOSPHATASE LOCUS AND BLOOD GROUP, HP, GM, AND INV LOCI. Am J Hum Genet (1965) 0.75