LSD and chromosomes.

Helicopters and medical emergencies. Br Med J (1968) 0.75

LSD and chromosomes. Br Med J (1968) 0.75

Characteristics of the BGM line of cells from African green monkey kidney. Brief report. Arch Gesamte Virusforsch (1970) 6.50

Mortality and reoperation after open and transurethral resection of the prostate for benign prostatic hyperplasia. N Engl J Med (1989) 3.97

Syndromes with cleft lip and cleft palate. Cleft Palate J (1978) 3.84

The airway: problems and predictions in 18,500 patients. Can J Anaesth (1994) 3.46

Registries and administrative data: organization and accuracy. Med Care (1993) 3.44

Reliability of the timeline follow-back sexual behavior interview. Ann Behav Med (1998) 3.15

Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluation. Am J Med Genet (1999) 3.02

The Proteus syndrome: the Elephant Man diagnosed. Br Med J (Clin Res Ed) (1986) 2.73

Establishment in continuous culture of a new type of lymphocyte from a "Burkitt like" malignant lymphoma (line D.G.-75). Int J Cancer (1977) 2.66

Predicting difficult intubation: a multivariable analysis. Can J Anaesth (2000) 2.41

In vivo and in vitro chromosomal damage induced by LSD-25. N Engl J Med (1967) 2.39

Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion. Humangenetik (1965) 2.37

Testing the raters: inter-rater reliability of standardized anaesthesia simulator performance. Can J Anaesth (1997) 2.37

Craniosynostoses: phenotypic/molecular correlations. Am J Med Genet (1995) 2.35

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. Am J Hum Genet (1997) 2.22

Colon and rectal anastomoses do not require routine drainage: a systematic review and meta-analysis. Ann Surg (1999) 2.20

Why is there no progress against cervical cancer? CMAJ (1996) 2.14

Is there a Baller-Gerold syndrome? Am J Med Genet (1996) 2.11

A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies. J Pediatr (1973) 1.98

Complementary therapies: have they become accepted in general practice? Med J Aust (2000) 1.98

The anesthetic record: accuracy and completeness. Can J Anaesth (1999) 1.96

Testing internal consistency and construct validity during evaluation of performance in a patient simulator. Anesth Analg (1998) 1.95

A newly recognized hamartomatous syndrome. Birth Defects Orig Artic Ser (1979) 1.89

Laparoscopic loop ileostomy for temporary fecal diversion. Dis Colon Rectum (1993) 1.88

Untoward reactions to lysergic acid diethylamide (LSD) resulting in hospitalization. N Engl J Med (1965) 1.87

Measuring patient satisfaction with anesthesia care: a review of current methodology. Anesth Analg (1998) 1.86

Analysis of phenotypic features and FGFR2 mutations in Apert syndrome. Am J Hum Genet (1995) 1.85

Comparing clinical information with claims data: some similarities and differences. J Clin Epidemiol (1991) 1.83

A survey of 112,000 anaesthetics at one teaching hospital (1975-83). Can Anaesth Soc J (1986) 1.81

The response of lymphocytes from non-immunized humans to antigen-antibody complexes. Clin Exp Immunol (1968) 1.79

The Saethre-Chotzen syndrome. Birth Defects Orig Artic Ser (1975) 1.72

Klippel-Trenaunay syndrome. Am J Med Genet (2000) 1.72

A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region. Hum Mol Genet (1997) 1.71

Bannayan-Riley-Ruvalcaba syndrome. Am J Med Genet (1992) 1.69

Craniosynostosis and syndromes with craniosynostosis: incidence, genetics, penetrance, variability, and new syndrome updating. Birth Defects Orig Artic Ser (1979) 1.67

Fanconi's anemia. Inherited susceptibility to chromosome breakage in various tissues. Ann Intern Med (1966) 1.67

Paternal trisomy 21 mosaicism and Down's syndrome. Am J Hum Genet (1971) 1.65

The incidence of airway problems depends on the definition used. Can J Anaesth (1996) 1.65

Holoprosencephaly and cytogenetic findings: further information. Am J Med Genet (1989) 1.63

Frontonasal dysplasia. J Pediatr (1970) 1.62

An etiologic and nosologic overview of craniosynostosis syndromes. Birth Defects Orig Artic Ser (1975) 1.62

Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome. Cytogenetics (1966) 1.62

The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography. Ann Genet (1971) 1.61

Studies on lysosomes. XII. Redistribution of acid hydrolases in human lymphocytes stimulated by phytohemagglutinin. J Cell Biol (1968) 1.58

Criminality in XYY and XXY men. Science (1976) 1.57

Trisomy 22: a clinical entity. J Pediatr (1971) 1.55

Tests of auditory-visual integration efficiency within the framework of the fuzzy logical model of perception. J Acoust Soc Am (2000) 1.55

Bayes factor of model selection validates FLMP. Psychon Bull Rev (2001) 1.55

Chromosomal damage in human leukocytes induced by lysergic acid diethylamide. Science (1967) 1.54

Stability of HL-A and appearance of other antigens (LIVA) at the surface of lymphoblasts grown in vitro. Haematologica (1969) 1.53

Pericentric inversion in a group D chromosome (13-15) associated with amenorrhea and gonadal dysgenesis. Ann Hum Genet (1967) 1.51

Perception of asynchronous and conflicting visual and auditory speech. J Acoust Soc Am (1996) 1.51

The premature infant: anesthesia for cesarean delivery. Anesth Analg (1994) 1.50

Critical respiratory events in the postanesthesia care unit. Patient, surgical, and anesthetic factors. Anesthesiology (1994) 1.49

Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome. Nat Genet (1996) 1.49

Variations in hysterectomy rates in Ontario: does the indication matter? CMAJ (1994) 1.48

Two human X-autosome translocations identified by autoradiography and fluorescence. Am J Hum Genet (1972) 1.48

Planned and unplanned postoperative admissions to critical care for mechanical ventilation. Can J Anaesth (1996) 1.48

The syndrome of ectrodactyly, ectodermal dysplasia and cleft lip and palate: report of a family demonstrating a dominant inheritance pattern. Clin Genet (1972) 1.42

Presence of gallstones is a poor indicator of the cause of obstructive jaundice. Surg Gynecol Obstet (1980) 1.41

Caffeine-stimulated acid and pepsin secretion: dose-response studies. Scand J Gastroenterol (1971) 1.39

Stimulation of mucus and nonparietal cell secretion by the E2 prostaglandins. Am J Dig Dis (1978) 1.39

Craniosynostosis in the Ullrich-Turner syndrome. Am J Med Genet (1990) 1.39

Chorionic villus sampling: the University of Maryland experience. Md Med J (1992) 1.38

Wiedemann-Beckwith syndrome, imprinting, IGF2, and H19: implications for hemihyperplasia, associated neoplasms, and overgrowth. Am J Med Genet (1994) 1.38

Appearance of hydrolase rich granules in human lymphocytes induced by phytohemagglutinin and antigens. Blood (1967) 1.35

Location of the genes for human heavy chain immunoglobulin to chromosome 6. Proc Natl Acad Sci U S A (1978) 1.35

Human dicentric Y chromosomes. Case report and review of the literature. J Med Genet (1973) 1.32

Fetal risk of anesthesia and surgery during pregnancy. Anesthesiology (1986) 1.31

The quest for meaningful outcomes. Anesthesiology (1993) 1.30

Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy. J Med Genet (1977) 1.30

DNA content measurements and an improved idiogram for the Indian muntjac. Cytometry (1993) 1.30

Accuracy of common hapatic duct size in the evaluation of extrahepatic biliary obstruction. Radiology (1980) 1.30

Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndrome. J Med Genet (1974) 1.29

Vinyl chloride exposure and human chromosome aberrations. Mutat Res (1975) 1.28

Confirmation of the regional localization of the genes for human acid alpha-glucosidase (GAA) and adenosine deaminase (ADA) by somatic cell hybridization. Ann Hum Genet (1984) 1.28

An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15. Ann Genet (1975) 1.28

Risk adjustment in claims-based research: the search for efficient approaches. J Clin Epidemiol (1989) 1.27

Precise identification of various chromosomal abnormalities. Ann Hum Genet (1973) 1.27

Sex-linked cleft palate. Report of a family and review of 77 kindreds. J Med Genet (1966) 1.26

Chromosomal localization of human haemoglobin structural genes. Nature (1972) 1.26

Ascorbic acid nutrition in gastroduodenal disorders. Br Med J (1967) 1.24

Stimulation of human tonsillar lymphocytes in vitro. Clin Exp Immunol (1966) 1.23

The oral manifestations of Apert syndrome. J Craniofac Genet Dev Biol (1992) 1.23

An update on the holoprosencephalic disorders. J Pediatr (1982) 1.22

A prospective study of the risk of developing multiple sclerosis in uncomplicated optic neuritis. Neurology (1979) 1.22

A multivariable model for predicting the need for blood transfusion in patients undergoing first-time elective coronary bypass graft surgery. Transfusion (2001) 1.21

64Cu metabolism in Menkes and normal cultured skin fibroblasts. Pediatr Res (1978) 1.21

Clinical differentiation between Proteus syndrome and hemihyperplasia: description of a distinct form of hemihyperplasia. Am J Med Genet (1998) 1.21

Racial differences in the length of the human Y chromosome. Cytogenetics (1966) 1.19

Genetic perspectives on craniosynostosis and syndromes with craniosynostosis. J Neurosurg (1977) 1.19

Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts. J Clin Invest (1978) 1.19

Holt-Oram syndrome: clinical and genetic study of a large family. Am J Hum Genet (1966) 1.18

Neonatal hepatitis and biliary atresia associated with trisomy 17-18 syndrome. N Engl J Med (1969) 1.17

Holoprosencephaly and facial dysmorphia: nosology, etiology and pathogenesis. Birth Defects Orig Artic Ser (1971) 1.17

Langer-Giedion syndrome. Birth Defects Orig Artic Ser (1974) 1.17

Chromatin-positive Klinefelter's syndrome with undetectable peripheral FSH levels. Am J Med (1975) 1.16

L-asparaginase and blastogenesis. Lancet (1969) 1.16