Published in Can J Public Health on November 20, 1975
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Monozygotic twinning and structural defects. J Pediatr (1979) 2.58
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Reinvestigation of oak leaf roller sex pheromone components and the hypothesis that they vary with diet. Science (1976) 2.44
Detection of nonintegrated plasmid deoxyribonucleic acid in the folded chromosome of Escherichia coli: physiochemical approach to studying the unit of segregation. J Bacteriol (1975) 2.43
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Incidence of inborn errors of metabolism in British Columbia, 1969-1996. Pediatrics (2000) 2.40
West Nile virus infection in mosquitoes, birds, horses, and humans, Staten Island, New York, 2000. Emerg Infect Dis (2001) 2.16
Congenital anomalies in American Indians of British Columbia. Genet Epidemiol (1986) 2.13
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Screening, counselling and treatment of hereditary metabolic disease; a survey of resources in Canada. Can Med Assoc J (1974) 2.11
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Errors of morphogenesis: concepts and terms. Recommendations of an international working group. J Pediatr (1982) 2.04
Cardiac arrhythmias during oral surgery with halothane-nitrous-oxide-oxygen anesthesia. JAMA (1969) 2.03
The combined use of a central registry and vital records for incidence studies of congenital defects. Br J Prev Soc Med (1968) 2.02
Down syndrome in British Columbia, 1952-73: incidence and mean maternal age. Teratology (1976) 1.89
Transcription of the 'non-transcribed' spacer of Drosophila melanogaster rDNA. Nucleic Acids Res (1983) 1.88
Progressive hemifacial atrophy (Parry-Romberg syndrome) report with review of genetics and nosology. Am J Med Genet (1983) 1.83
A diagnostic schema for identifying enterobacteriaceae and miscellaneous gram-negative bacilli. Am J Clin Pathol (1969) 1.80
A pseudogene structure in 5S DNA of Xenopus laevis. Cell (1977) 1.67
Motor neuron disease and amyotrophic lateral sclerosis: relation of high CSF protein content to paraproteinemia and clinical syndromes. Neurology (1990) 1.61
Isolation and expression of a new mouse homeobox gene. Development (1988) 1.59
Cataracts, microcephaly, kyphosis, and limited joint movement in two siblings: a new syndrome. J Pediatr (1971) 1.56
Fine needle aspiration in the diagnosis of metastatic melanoma. J Am Acad Dermatol (2000) 1.56
Intramolecular long-distance electron transfer in organic molecules. Science (1988) 1.54
Lead absorption in indoor firing range users. Am J Public Health (1989) 1.54
Inheritance of tuberous sclerosis. Lancet (1979) 1.52
Nonintegrated plasmid-chromosome complexes in Escherichia coli. J Bacteriol (1976) 1.47
Clinical and genetic aspects of seizure disorders prevalent in an isolated African population. Epilepsia (1979) 1.46
Borderline normal intelligence in the Smith-Lemli-Opitz (RSH) syndrome. Am J Med Genet (1980) 1.45
Cloning, characterization, and expression in Escherichia coli of the Streptomyces clavuligerus gene encoding deacetoxycephalosporin C synthetase. J Bacteriol (1989) 1.44
Progressive multifocal leukoencephalopathy in a male homosexual with T-cell immune deficiency. N Engl J Med (1982) 1.41
Homoeobox gene expression in mouse embryos varies with position by the primitive streak stage. Nature (1987) 1.41
Ovipositional site selection by Anopheles gambiae: influences of substrate moisture and texture. Med Vet Entomol (2005) 1.40
Child automobile restraints: evaluation of health education. Pediatrics (1977) 1.37
A new dominant gene mental retardation syndrome. Association with small stature, tapering fingers, characteristic facies, and possible hydrocephalus. Am J Dis Child (1971) 1.36
Relative frequency of the Hurler and Hunter syndromes. N Engl J Med (1971) 1.35
Toxicity of bloodmeals from ivermectin-treated cattle to Anopheles gambiae s.l. Ann Trop Med Parasitol (2009) 1.34
Secretion of staphylococcal nuclease by Bacillus subtilis. J Bacteriol (1985) 1.34
Clinical and ultrastructural heterogeneity of type IV Ehlers-Danlos syndrome. Hum Genet (1979) 1.31
Vegetation stress detection through chlorophyll a + b estimation and fluorescence effects on hyperspectral imagery. J Environ Qual (2002) 1.30
Is there a correction mechanism in the 5S multigene system? Nature (1978) 1.30
Broad thumbs and toes and mental retardation. Unusual dermatoglyphic observations in two individuals. Am J Dis Child (1966) 1.29
Incidence rates for cleft lip and palate in British Columbia 1952-71 for North American Indian, Japanese, Chinese and total populations: secular trends over twenty years. Teratology (1977) 1.28
Poland syndrome in British Columbia: incidence and reproductive experience of affected persons. Am J Med Genet (1977) 1.27
Development of IgE and allergy in infancy. J Allergy Clin Immunol (1975) 1.25
Partial characterization of nucleoids and nucleoid-plasmid complexes from Salmonella typhimurium. J Bacteriol (1976) 1.23
Editorial comment: variability in the Smith-Lemli-Opitz syndrome: overlap with the Meckel syndrome. Am J Med Genet (1983) 1.21
[The campomelic syndrome]. Presse Med (1971) 1.21
Prolonged intracerebral infection with poliovirus in asymptomatic mice. Ann Neurol (1981) 1.21
Kinetics and pool size of primary bile acids in man. Gastroenterology (1971) 1.20
Dermatoglyphics in pediatric practice. J Pediatr (1966) 1.19
Secretion and processing of staphylococcal nuclease by Bacillus subtilis. J Bacteriol (1987) 1.19
R-factor responsible for an outbreak of multiply antibiotic-resistant Klebsiella pneumoniae. Antimicrob Agents Chemother (1980) 1.19
Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome. Am J Med Genet (1988) 1.18
The beta-lactam biosynthesis genes for isopenicillin N epimerase and deacetoxycephalosporin C synthetase are expressed from a single transcript in Streptomyces clavuligerus. J Bacteriol (1990) 1.17
Dermatoglyphics of the broad thumb and great toe syndrome. Am J Dis Child (1967) 1.17
Micrognathia, polydactyly, and cleft palate. J Pediatr (1968) 1.15
Structurally related receptors and antagonists compete for secreted Wnt ligands. Cell (1997) 1.15
Detoxification enzyme differences between a herbivorous and predatory mite. Science (1982) 1.13
A transcriptionally active pseudogene in xenopus laevis oocyte 5S DNA. Cell (1981) 1.12
Stereochemistry of the hydrolysis products and their acetonides of two stereoisomeric benzo[a]pyrene 7,8-diol 9,10-epoxides. J Am Chem Soc (1977) 1.12
A cluster of transfusion-associated babesiosis cases traced to a single asymptomatic donor. JAMA (1999) 1.11
Incidence and genetics of Legg-Perthes disease (osteochondritis deformans) in British Columbia: evidence of polygenic determination. J Med Genet (1972) 1.10
Inhibition of Tcf3 binding by I-mfa domain proteins. Mol Cell Biol (2001) 1.10
Cloning and sequencing of the beta-lactam hydroxylase gene (cefF) from Streptomyces clavuligerus: gene duplication may have led to separate hydroxylase and expandase activities in the actinomycetes. J Bacteriol (1991) 1.09
Neuropathology of systemic circulatory arrest in adult monkeys. Neurology (1972) 1.09
Hutterite cerebro-osteo-nephrodysplasia: autosomal recessive trait in a Lehrerleut Hutterite family from Montana. Am J Med Genet (1985) 1.08
Membrane-tethered Drosophila Armadillo cannot transduce Wingless signal on its own. Development (1999) 1.08
Hypospadias in successive generations - possible dominant gene inheritance. Clin Genet (1976) 1.08
Birth prevalence and recurrence rates of neural tube defects in southern Alberta in 1970-81. CMAJ (1988) 1.07
Host specificity of filamentous, segmented microorganisms adherent to the small bowel epithelium in mice and rats. Appl Environ Microbiol (1984) 1.07
An update on the frequency of mucopolysaccharide syndromes in British Columbia. Hum Genet (1990) 1.06
Pungent spices, ground red pepper, and synthetic capsaicin as onion fly ovipositional deterrents. J Chem Ecol (1989) 1.06
A new complication of AIDS: thoracic myelitis caused by herpes simplex virus. Neurology (1985) 1.06
Reproductive counseling in patients who have had a spontaneous abortion. Am J Obstet Gynecol (1977) 1.06
The Nagar syndrome (acrofacial dysostosis): evidence for autosomal dominant inheritance. Birth Defects Orig Artic Ser (1977) 1.05
Some epidemiological aspects of Down's syndrome in British Columbia. Br J Prev Soc Med (1968) 1.05
X-linked mental retardation with macro-orchidism and marker-X chromosomes. Am J Med Genet (1980) 1.05
Molecular characterization of the acyl-coenzyme A:isopenicillin N acyltransferase gene (penDE) from Penicillium chrysogenum and Aspergillus nidulans and activity of recombinant enzyme in Escherichia coli. J Bacteriol (1990) 1.05
Hereditary brachydactyly and hip disease. Unusual radiological and dermatoglyphic findings in a kindred. J Pediatr (1968) 1.04
ABO incompatibility as a cause of spontaneous abortion: evidence from abortuses. J Med Genet (1972) 1.04
Zyme, a novel and potentially amyloidogenic enzyme cDNA isolated from Alzheimer's disease brain. J Biol Chem (1997) 1.04
Apparent validity of alternative survey methods. J Community Health (1979) 1.04
Double aneuploidy: the frequency of XXY in males with Down's syndrome. Am J Hum Genet (1969) 1.04