Published in Lancet on April 20, 1974
Neurodevelopment of children exposed in utero to phenytoin and carbamazepine monotherapy. JAMA (1994) 2.82
The impact of two-dimensional versus three-dimensional ultrasound exposure on maternal-fetal attachment and maternal health behavior in pregnancy. Ultrasound Obstet Gynecol (2006) 2.65
Elevated matrix metalloprotease and angiostatin levels in integrin alpha 1 knockout mice cause reduced tumor vascularization. Proc Natl Acad Sci U S A (2000) 2.46
The chromosome constitution of 1000 human spermatozoa. Hum Genet (1983) 2.21
Neurodevelopment of children exposed in utero to antidepressant drugs. N Engl J Med (1997) 2.21
Activin/inhibin beta B subunit gene disruption leads to defects in eyelid development and female reproduction. Genes Dev (1994) 1.91
Maternal serum alpha-fetoprotein screening: report of a Canadian pilot project. CMAJ (1987) 1.72
Integrin alpha1beta1 mediates a unique collagen-dependent proliferation pathway in vivo. J Cell Biol (1998) 1.54
A case of ring (9)/del(9p) mosaicism associated with gastroesophageal reflux. Am J Med Genet (1988) 1.47
Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1. Am J Hum Genet (1998) 1.44
Treatment of murine lupus with cDNA encoding IFN-gammaR/Fc. J Clin Invest (2000) 1.40
Cardiovascular effects of peritoneal insufflation of carbon dioxide for laparoscopy. Br Med J (1971) 1.35
Craniosynostosis. II. Coronal synostosis: its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactyly. Teratology (1977) 1.33
Craniosynostosis. I. Sagittal synostosis: its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s). Teratology (1976) 1.33
Caridac output and arterial blood-gas tension during laparoscopy. Br J Anaesth (1972) 1.32
Pregnancy complications in type IV Ehlers-Danlos Syndrome. Lancet (1983) 1.16
Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother. J Med Genet (1980) 1.10
So you want to have the baby at home? CMAJ (1989) 1.07
Nonimmunologic hydrops fetalis. Am J Obstet Gynecol (1984) 1.05
Prenatal diagnosis and management of congenital defects of the anterior abdominal wall. Am J Obstet Gynecol (1987) 1.05
Effectiveness of a pregnancy smoking cessation program. J Obstet Gynecol Neonatal Nurs (1992) 1.04
Expression of matrix metalloprotease-2-cleaved laminin-5 in breast remodeling stimulated by sex steroids. Am J Pathol (1999) 1.01
Autosomal dominant anterior polar cataracts associated with a familial 2;14 translocation. J Med Genet (1984) 0.98
Trigonocephaly and associated minor anomalies in mother and son. J Med Genet (1976) 0.95
Trisomy 18 and cyclopia. Teratology (1976) 0.95
Multiple karyotypic changes in retinoblastoma tumor cells: presence of normal chromosome No. 13 in most tumors. Cancer Genet Cytogenet (1982) 0.94
A dominantly inherited cytogenetic anomaly: a possible cell division mutant. Hum Genet (1983) 0.94
Sacrococcygeal teratoma: prenatal diagnosis and management. Am J Obstet Gynecol (1987) 0.94
Familial retinoblastoma: segregation of chromosome 13 in four families. Am J Hum Genet (1980) 0.93
Composition of the amniotic fluid and maternal serum in pregnancy. Am J Obstet Gynecol (1974) 0.93
The cloned butyrylcholinesterase (BCHE) gene maps to a single chromosome site, 3q26. Genomics (1991) 0.92
Amniotic fluid tests for fetal maturity. Am J Obstet Gynecol (1974) 0.91
Gene deletion and duplication effects on phenotype and gamma globulin levels. J Med Genet (1971) 0.90
The very dense granule in rabbit platelets. J Ultrastruct Res (1968) 0.89
Partial trisomy 20 confirmed by gene dosage studies. Am J Med Genet (1979) 0.88
Amniotic fluid testosterone in the prenatal determination of fetal sex. Am J Obstet Gynecol (1977) 0.87
Mixed teratoid tumors of the liver and neck in trisomy 13. Am J Clin Pathol (1978) 0.86
Use of ultrasound for placental localization in genetic amniocentesis. Obstet Gynecol (1974) 0.85
Letter: Amniotic fluid on maternal urine? Lancet (1976) 0.84
IgA and partial deletions of chromosome 18. Lancet (1969) 0.84
Natural history of placenta previa ascertained by diagnostic ultrasound. Am J Obstet Gynecol (1979) 0.84
Prenatal ultrasonic diagnosis of occipital encephalocele. Am J Obstet Gynecol (1978) 0.84
Segregation of chromosome 13 in retinoblastoma. Lancet (1978) 0.84
Mosaicism in amniotic fluid cell cultures. Birth Defects Orig Artic Ser (1977) 0.83
Kinetochore immunofluorescence in micronuclei: a rapid method for the in situ detection of aneuploidy and chromosome breakage in human fibroblasts. Mutat Res (1988) 0.83
Alterations in DMBA-induced rat mammary tumors by actinomycin D. J Natl Cancer Inst (1973) 0.83
Maxillonasal dysplasia (Binder's syndrome). Plast Reconstr Surg (1979) 0.83
Prenatal diagnosis of hypophosphatasia. N Engl J Med (1976) 0.82
Amniotic fluid tests for fetal maturity in normal and abnormal pregnancies. Am J Obstet Gynecol (1976) 0.82
Sex chromosome mosaicism not detected at amniocentesis. Prenat Diagn (1990) 0.82
Prenatal diagnosis by fetoscopy with subsequent normal delivery: report of a case. Am J Obstet Gynecol (1976) 0.82
Prenatal diagnosis of hypophosphatasia. Birth Defects Orig Artic Ser (1976) 0.81
The "fetoscope"--a new clinical tool for prenatal genetic diagnosis. Am J Obstet Gynecol (1975) 0.81
Chorionic villus sampling: the need for further assessment. CMAJ (1986) 0.81
Balanced complex chromosome rearrangement ascertained through prenatal diagnosis. Am J Med Genet (1994) 0.81
Amniotic fluid lecithin/sphingomyelin ratio, palmitic acid, palmitic acid/stearic acid ratio, total cortisol, creatinine, and percentage of lipid-positive cells in assessment of fetal maturity and fetal pulmonary maturity: a comparison. Am J Obstet Gynecol (1979) 0.80
A de novo case of trisomy 10p: gene dosage studies of hexokinase, inorganic pyrophosphatase and adenosine kinase. Hum Genet (1984) 0.80
Fetal cystic hygroma colli: antenatal diagnosis, significance, and management. Am J Obstet Gynecol (1986) 0.80
What information on fetal anatomy can be provided by a single first-trimester transabdominal three-dimensional sweep? Ultrasound Obstet Gynecol (2008) 0.80
An X;9 translocation, primary amenorrhea, and hypothalamic dysfunction. Am J Med Genet (1983) 0.80
The antenatal diagnosis of genetic disease. Am J Obstet Gynecol (1974) 0.80
The 4p- syndrome--an autopsy study. Hum Pathol (1980) 0.79
Amniotic band syndrome causing fetal head deformity. Prenat Diagn (1985) 0.79
Fetoscopy in prenatal diagnosis of the Majewski and the Saldino-Noonan types of the Short Rib-Polydactyly syndromes. Clin Genet (1984) 0.79
The buccal smear: Reassessment of its usefulness. Can Med Assoc J (1976) 0.79
Verbal deficits in Klinefelter (XXY) adults living in the community. Clin Genet (1988) 0.79
Therapy-related leukemia and myelodysplasia in small-cell lung cancer. Report of a case and results of morphologic, cytogenetic, and bone marrow culture studies in long-term survivors. Arch Intern Med (1986) 0.78
Fetoscopy and anterior placentas. N Engl J Med (1977) 0.78
Smaller fetal thymuses in pre-eclampsia: a prospective cross-sectional study. Ultrasound Obstet Gynecol (2011) 0.78
Prenatal demonstration of a cervical myelocystocele. Prenat Diagn (1992) 0.78
Expression of human choriogonadotropin-like material correlates with metastatic phenotype of R3230 AC rat adenocarcinoma. Cancer Invest (1987) 0.78
The otolaryngologist as genetic counselor. Otolaryngol Clin North Am (1981) 0.78
A possible primidone embryopathy. J Pediatr (1979) 0.78
Infant outcome following mid-trimester amniocentesis: development and physical status at age six months. Br J Obstet Gynaecol (1985) 0.78
A 'new' syndrome of mental retardation with characteristic facies and brachyphalangy. J Med Genet (1977) 0.78
Hypertonic saline as an abortifacient in a select group of patients. Obstet Gynecol (1983) 0.77
Genetic amniocentesis in seventy twin pregnancies. Am J Obstet Gynecol (1984) 0.77
Werner's syndrome. Lancet (1970) 0.76
Werner's syndrome and acute myeloid leukemia. Can Med Assoc J (1971) 0.76
Fetal therapy. Baillieres Clin Obstet Gynaecol (1991) 0.76
Studies on the action of interleukin-1 on term human fetal membranes and decidua. Can J Physiol Pharmacol (1994) 0.75
Isochromosome for the long arm of the Y in an infertile male. Hum Genet (1978) 0.75
Antenatal genetic diagnosis: current status and future prospects. Can Med Assoc J (1979) 0.75
Valproic acid therapy and neural tube defects. Can Med Assoc J (1985) 0.75
Medical advocacy for the oppressed. Lancet (1998) 0.75
Variation in chromosome 19. J Med Genet (1979) 0.75
Males with chronic myeloid leukemia and the 45, XO, Ph1 chromosome pattern. Can Med Assoc J (1974) 0.75
Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative study. Genet Med (2001) 0.75
Endocrine, cytogenetic and psychometric features of patients with X-isochromosome 46, X, i(Xq) Turner's syndrome: a preliminary study in nine patients. Clin Invest Med (1984) 0.75
A further case of Philadelphia chromosome-positive chronic myeloid leukemia with t(3;9;22) Cancer Genet Cytogenet (1988) 0.75
Mosaicism for a small marker chromosome resulting from a familial Robertsonian translocation (21;22). Clin Genet (1999) 0.75
Glucocorticoid-dependent transformation by human papillomavirus type 16 E7 coding and 3' noncoding sequences. Virology (1992) 0.75
The changing role of the pathologist. CMAJ (1997) 0.75
Prenatal diagnosis of del(11)(p13p15). Prenat Diagn (1988) 0.75