Published in Birth Defects Orig Artic Ser on January 01, 1977
Characteristics of the BGM line of cells from African green monkey kidney. Brief report. Arch Gesamte Virusforsch (1970) 6.50
Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation. Hum Mol Genet (1998) 4.72
Nevoid basal-cell carcinoma syndrome. Medicine (Baltimore) (1987) 4.60
Germline mutations in PTEN are present in Bannayan-Zonana syndrome. Nat Genet (1997) 4.39
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
Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease. Hum Mol Genet (1997) 3.56
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
Multiple lentigenes syndrome. Am J Dis Child (1969) 3.39
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. Hum Mol Genet (1999) 3.22
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
Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes. Lancet (2001) 2.77
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
Calcifying odontogenic cyst. Range, variations and neoplastic potential. Acta Odontol Scand (1981) 2.45
Predicting difficult intubation: a multivariable analysis. Can J Anaesth (2000) 2.41
Solitary maxillary central incisor and short stature. J Pediatr (1977) 2.41
In vivo and in vitro chromosomal damage induced by LSD-25. N Engl J Med (1967) 2.39
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
The syndrome of pits of the lower lip and cleft lip and/or palate. Genetic considerations. Am J Hum Genet (1967) 2.32
In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome. J Med Genet (2003) 2.26
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 human chondrodysplasia due to a mutation in a TGF-beta superfamily member. Nat Genet (1996) 2.11
Urofacial (ochoa) syndrome. Am J Med Genet (1987) 2.03
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
Melanotic neuroectodermal tumor of infancy--a neoplasm of neural crese origin. Report of a case associated with high urinary excretion of vanilmandelic acid. Cancer (1966) 1.98
The anesthetic record: accuracy and completeness. Can J Anaesth (1999) 1.96
Successful bone-marrow transplantation for infantile malignant osteopetrosis. N Engl J Med (1980) 1.95
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
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
Classification and birth prevalence of orofacial clefts. Am J Med Genet (1998) 1.83
Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK. Am J Hum Genet (2001) 1.81
A survey of 112,000 anaesthetics at one teaching hospital (1975-83). Can Anaesth Soc J (1986) 1.81
Multiple hamartoma syndrome (Cowden's disease). Arch Dermatol (1972) 1.79
The tricho-rhino-phalangeal syndrome with exostoses (or Langer-Giedion syndrome): four additional patients without mental retardation and review of the literature. Am J Med Genet (1984) 1.77
Robin's syndrome. A probably X-linked recessive subvariety exhibiting persistence of left superior vena cava and atrial septal defect. Am J Dis Child (1970) 1.76
The Saethre-Chotzen syndrome. Birth Defects Orig Artic Ser (1975) 1.72
Klippel-Trenaunay syndrome. Am J Med Genet (2000) 1.72
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
Oral-facial-digital syndrome type VI (Váradi syndrome): further clinical delineation. Am J Med Genet (1990) 1.66
Pseudo-trisomy 13 syndrome. Am J Med Genet (1991) 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
Noonan-like/multiple giant cell lesion syndrome. Am J Med Genet (1991) 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
Popliteal pterygium syndrome . A syndrome comprising cleft lip-palate, popliteal and intercrural pterygia, digital and genital anomalies. Pediatrics (1968) 1.62
The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography. Ann Genet (1971) 1.61
Bayes factor of model selection validates FLMP. Psychon Bull Rev (2001) 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
Coliphages as ecological indicators of enteroviruses in various water systems. Bull World Health Organ (1981) 1.55
Chromosomal damage in human leukocytes induced by lysergic acid diethylamide. Science (1967) 1.54
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
Leukoplakia, lichen planus, and other oral keratoses in 23,616 white Americans over the age of 35 years. Oral Surg Oral Med Oral Pathol (1986) 1.47
Patterns of DNA replication of human chromosomes. II. Replication map and replication model. Am J Hum Genet (1982) 1.45
Double dens invaginatus of molarized maxillary central incisors, premolarization of maxillary lateral incisors, multituberculism of the mandibular incisors, canines and first premolar, and sensorineural hearing loss. Clin Dysmorphol (1992) 1.43
Pycnodysostosis. Clinical and genetic considerations. Am J Dis Child (1968) 1.43
Multiple mucosal neuromas, pheochromocytoma and medullary carcinoma of the thyroid--a syndrome. Cancer (1968) 1.41
Presence of gallstones is a poor indicator of the cause of obstructive jaundice. Surg Gynecol Obstet (1980) 1.41
Familial occurrence of mesiodens. Oral Surg Oral Med Oral Pathol (1969) 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
Wiedemann-Beckwith syndrome, imprinting, IGF2, and H19: implications for hemihyperplasia, associated neoplasms, and overgrowth. Am J Med Genet (1994) 1.38
Chorionic villus sampling: the University of Maryland experience. Md Med J (1992) 1.38
Acrodysostosis. A syndrome of peripheral dysostosis, nasal hypoplasia, and mental retardation. Am J Dis Child (1971) 1.38
Hypohidrotic ectodermal dysplasia in females. A critical analysis and argument for genetic heterogeneity. Z Kinderheilkd (1970) 1.38
Malformation syndromes. A selected miscellany. Birth Defects Orig Artic Ser (1975) 1.35
Diagnosis of craniofacial anomalies: subjective evaluation--Gestalt. Birth Defects Orig Artic Ser (1980) 1.35
A two-hit model for developmental defects in Gorlin syndrome. Nat Genet (1996) 1.35
Growth retardation, alopecia, pseudo-anodontia, and optic atrophy--the GAPO syndrome: report of a patient and review of the literature. Am J Med Genet (1984) 1.32
Human dicentric Y chromosomes. Case report and review of the literature. J Med Genet (1973) 1.32
Cranio-carop-tarsal dysplasia or the whistling face syndrome. I. Clinical considerations. Am J Dis Child (1969) 1.31
Fetal risk of anesthesia and surgery during pregnancy. Anesthesiology (1986) 1.31