Published in Obstet Gynecol on August 01, 1982
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An automated "high-pressure" liquid-chromatographic assay for hemoglobin A1c. Clin Chem (1984) 1.27
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Coupling between oxidation state and hydrogen bond conformation in heme proteins. Proc Natl Acad Sci U S A (1979) 1.15
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Prenatal diagnosis and management of congenital defects of the anterior abdominal wall. Am J Obstet Gynecol (1987) 1.05
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Application of special diagnostic techniques in the management of nodular goitre. Can Med Assoc J (1976) 1.01
Distal arthrogryposis type II: a family with varying congenital abnormalities. Am J Med Genet (1986) 1.00
Asymmetry and skin pigmentary anomalies in chromosome mosaicism. J Med Genet (1994) 1.00
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New estimates of Down syndrome risks at chorionic villus sampling, amniocentesis, and livebirth in women of advanced maternal age from a uniquely defined population. Prenat Diagn (1995) 0.96
Trigonocephaly and associated minor anomalies in mother and son. J Med Genet (1976) 0.95
Massive pulmonary hemorrhage as a presenting feature in congenital hyperammonemia. J Pediatr (1976) 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
Composition of the amniotic fluid and maternal serum in pregnancy. Am J Obstet Gynecol (1974) 0.93
B-mode ultrasonic examination of the testes. J Clin Ultrasound (1974) 0.93
Treatable complications in undiagnosed cases of autosomal dominant polycystic kidney disease. Lancet (1991) 0.93
Importance of complete follow-up of spontaneous fetal loss after amniocentesis and chorion villus sampling. Lancet (1992) 0.92
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Partial trisomy 20 confirmed by gene dosage studies. Am J Med Genet (1979) 0.88
Results of a double-blind controlled study on the use of betamethasone in the prevention of respiratory distress syndrome. Am J Obstet Gynecol (1980) 0.88
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Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications. Mol Syndromol (2011) 0.87
Amniotic fluid testosterone in the prenatal determination of fetal sex. Am J Obstet Gynecol (1977) 0.87
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Hazards of prenatal detection of neural-tube defects by screening maternal serum for alpha-fetoprotein. Can Med Assoc J (1978) 0.86
Expression of the somatostatin receptor subtype-2 gene predicts response of human pancreatic cancer to octreotide. Surgery (1996) 0.85
Use of ultrasound for placental localization in genetic amniocentesis. Obstet Gynecol (1974) 0.85
Prenatal ultrasonic diagnosis of occipital encephalocele. Am J Obstet Gynecol (1978) 0.84
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The application of ultrasound to the study of thyroid enlargement: management of 450 cases. Arch Surg (1975) 0.84
IgA and partial deletions of chromosome 18. Lancet (1969) 0.84
Congenital microcephaly due to vascular disruption: in utero documentation. Pediatrics (1986) 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
More on cephalosporin interference with creatinine determinations. Clin Chem (1982) 0.83
Mosaicism in amniotic fluid cell cultures. Birth Defects Orig Artic Ser (1977) 0.83
Maxillonasal dysplasia (Binder's syndrome). Plast Reconstr Surg (1979) 0.83
Amniotic fluid tests for fetal maturity in normal and abnormal pregnancies. Am J Obstet Gynecol (1976) 0.82
Amniotic fluid spectrophotometry, urinary estrogen estimations, and intrauterine transfusion in severe Rh isoimmunization. Am J Obstet Gynecol (1968) 0.82
Prenatal diagnosis by fetoscopy with subsequent normal delivery: report of a case. Am J Obstet Gynecol (1976) 0.82
Factors in a woman's decision to undergo genetic amniocentesis for advanced maternal age. Nurs Res (1982) 0.82
Presymptomatic testing for myotonic dystrophy by means of the linked DNA marker APOC2. Med J Aust (1988) 0.82
Weights of fetuses with autosomal trisomies at termination of pregnancy: an investigation of the etiologic factors of low serum alpha-fetoprotein values. Am J Obstet Gynecol (1988) 0.82
Sex chromosome mosaicism not detected at amniocentesis. Prenat Diagn (1990) 0.82
Prenatal diagnosis of hypophosphatasia. N Engl J Med (1976) 0.82
Prenatal diagnosis of hypophosphatasia. Birth Defects Orig Artic Ser (1976) 0.81