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The associations of nuchal translucency and fetal abnormalities; significance and implications. J Clin Diagn Res (2013) 0.81

Web-neck anomaly and its association with congenital heart disease. Am J Med Genet (1996) 0.75

Incidence of fetal alcohol syndrome and prevalence of alcohol-related neurodevelopmental disorder. Teratology (1997) 4.86

The effects of moderate alcohol consumption during pregnancy on fetal growth and morphogenesis. J Pediatr (1978) 2.72

The association of waterborne chloroform with intrauterine growth retardation. Epidemiology (1992) 2.10

Risks to the offspring of women treated with hydantoin anticonvulsants, with emphasis on the fetal hydantoin syndrome. J Pediatr (1976) 2.00

Prenatal cocaine exposure and fetal vascular disruption. Pediatrics (1990) 1.97

The fetal hydantoin syndrome. J Pediatr (1975) 1.80

Deletions of different segments of the long arm of chromosome 4. Am J Med Genet (1981) 1.72

Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome. J Pediatr (1983) 1.68

Terbutaline pump maintenance therapy for prevention of preterm delivery: a double-blind trial. Am J Obstet Gynecol (1998) 1.60

Magnetic resonance imaging of brain anomalies in fetal alcohol syndrome. Pediatrics (1997) 1.59

Can prenatal ultrasound findings predict ambulatory status in fetuses with open spina bifida? Am J Obstet Gynecol (2001) 1.55

Holoprosencephaly in infants of diabetic mothers. J Pediatr (1983) 1.51

Oculodentodigital dysplasia. Four new reports and a literature review. Arch Ophthalmol (1979) 1.50

Assessment of reproductive disorders and birth defects in communities near hazardous chemical sites. I. Birth defects and developmental disorders. Reprod Toxicol (1997) 1.50

Autosomal recessive cerebellar hypoplasia. J Child Neurol (1989) 1.49

Anesthetic management of a parturient with Eisenmenger's syndrome. Anesth Analg (1990) 1.48

Management of fetal hemolytic disease by cordocentesis. I. Prediction of fetal anemia. Am J Obstet Gynecol (1991) 1.43

Fetal alcohol syndrome. Experience with 41 patients. JAMA (1976) 1.39

Saethre-Chotzen syndrome: a broad and variable pattern of skeletal malformations. J Pediatr (1977) 1.35

Small structural changes of chromosome 8. Two cases with evidence for deletion. Hum Genet (1977) 1.28

Criteria for identifying and listing substances known to cause developmental toxicity under California's Proposition 65. Reprod Toxicol (1989) 1.20

Letter: Incidence of conjoined twinning. Lancet (1975) 1.16

Summary of workshop: early discharge and neonatal hyperbilirubinemia. Pediatrics (1995) 1.15

Further delineation of Weaver syndrome. J Pediatr (1986) 1.15

U-shaped palatal defect in the Robin anomalad: developmental and clinical relevance. J Pediatr (1975) 1.13

Psychometric studies in muscular dystrophy type 3a (Duchenne). Dev Med Child Neurol (1967) 1.13

The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigations. Eur J Epidemiol (1998) 1.10

Comorbidity of 5,10-methylenetetrahydrofolate reductase and methionine synthase gene polymorphisms and risk for neural tube defects. J Med Genet (2000) 1.04

Helmet treatment for plagiocephaly and congenital muscular torticollis. J Pediatr (1979) 1.02

Teratogen update: fetal hydantoin effects. Teratology (1986) 1.00

Management of fetal hemolytic disease by cordocentesis. II. Outcome of treatment. Am J Obstet Gynecol (1991) 0.97

A five-year statewide experience with congenital diaphragmatic hernia. Am J Obstet Gynecol (1991) 0.96

The iduronidase-deficient mucopolysaccharidoses: clinical and roentgenorgraphic features. Pediatrics (1976) 0.96

Shprintzen-Goldberg syndrome: a clinical analysis. Am J Med Genet (1998) 0.95

Independent dysmorphology evaluations at birth and 4 years of age for children exposed to varying amounts of alcohol in utero. Pediatrics (1988) 0.94

Trisomy 3 (p23-pter) resulting from maternal translocation, t (3 ; 4)(p23 ; q35). Ann Genet (1978) 0.94

Palpebral fissure size in newborn infants. J Pediatr (1978) 0.93

First report of mosaic trisomy 12 in a liveborn individual. Am J Med Genet (1983) 0.90

The fetal alcohol syndrome: clinical delineation. Ann N Y Acad Sci (1976) 0.90

Spray adhesives and birth defects. JAMA (1976) 0.90

Subtotal neonatal calvariectomy for severe craniosynostosis. J Pediatr (1977) 0.89

Purification and characterization of chicken erythrocyte ferrochelatase. Biochem J (1984) 0.88

The fetal trimethadione syndrome. J Pediatr (1975) 0.88

Perspectives on the cause and frequency of the fetal alcohol syndrome. Ann N Y Acad Sci (1976) 0.87

Börjeson-Forssman-Lehmann syndrome: further delineation in five cases. Am J Med Genet (1984) 0.87

Value of perinatal autopsy. Obstet Gynecol (1999) 0.86

Prominent lateral palatine ridges: developmental and clinical relevance. J Pediatr (1976) 0.86

Dominantly inherited dilated cardiomyopathy. Am J Med Genet (1987) 0.85

Partial 8p- syndrome. J Genet Hum (1980) 0.85

Factors influencing maternal estimates of genetic risk. Am J Med Genet (1985) 0.85

Pentasomy X with multiple dislocations. Am J Med Genet (1979) 0.84

Ocular and systemic manifestations of Stickler's syndrome: a preliminary report. Birth Defects Orig Artic Ser (1982) 0.84

Second-trimester cystic hygroma: prognosis of septated and nonseptated lesions. Obstet Gynecol (1996) 0.84

Fetal injury with midtrimester diagnostic amniocentesis. Obstet Gynecol (1979) 0.83

Slowly progressive X-linked recessive muscular dystrophy (type 3b). Report of cases and review of the literature. Arch Intern Med (1967) 0.82

Changes in frequencies of heterozygous thermolabile 5,10-methylenetetrahydrofolate reductase gene in fetuses with neural tube defects. J Med Genet (2002) 0.82

Clinical management issues in males with sex chromosomal mosaicism and discordant phenotype/sex chromosomal patterns. Clin Pediatr (Phila) (1991) 0.82

Potential human teratogenicity of frequently prescribed drugs. Obstet Gynecol (1990) 0.80

The association between fetal karyotype and mean corpuscular volume. Am J Obstet Gynecol (1991) 0.80

Alcohol and the fetus. Br J Hosp Med (1977) 0.79

Gastric bypass surgery as maternal risk factor for neural tube defects. Lancet (1988) 0.79

Hydramnios prediction of adverse perinatal outcome. Obstet Gynecol (1999) 0.79

Fetal hydantoin syndrome: current status. J Pediatr (1982) 0.79

Fetal hydantoin syndrome. Lancet (1976) 0.78

Amniotic fluid embolism after saline amnioinfusion: two cases and review of the literature. Obstet Gynecol (1994) 0.78

Fetal echogenic bowel on ultrasound: is there clinical significance? Fetal Diagn Ther (1994) 0.78

Letter: Haloperidol and limb deformity. JAMA (1975) 0.77

Antenatal screening for factor V Leiden mutation: a critical appraisal. Obstet Gynecol (1997) 0.77

Craniofacial development in myotonic dystrophy. Cleft Palate Craniofac J (1992) 0.77

Ultrasound findings and multiple marker screening in trisomy 18. Obstet Gynecol (2000) 0.76

A teratologist to extinction. Ad Hoc Committee on Grant Funding. Teratology (1996) 0.75

Pregnancy outcomes following false-positive multiple marker screening tests. Am J Perinatol (1997) 0.75

Midtrimester selective delivery of an acardiac twin. Am J Obstet Gynecol (1993) 0.75

Risk factors for cordocentesis and fetal intravascular transfusion. Am J Obstet Gynecol (1991) 0.75

Syndrome identification case report 101: loose, redundant skin, craniofacial defects, and hypotonia. J Clin Dysmorphol (1983) 0.75

The Summitt syndrome: observations on a third case. Am J Med Genet (1979) 0.75

The muscular dystrophies in Iowa. J Iowa Med Soc (1968) 0.75

Fortuitous detection of a sporadic carrier of Duchenne's muscular dystrophy. Humangenetik (1968) 0.75

Maternal exposure to spermicides in relation to certain birth defects. N Engl J Med (1987) 0.75

Unique phenotype associated with a pericentric inversion of chromosome 6 in three generations. Am J Med Genet (1991) 0.75

Elevated amniotic fluid ferritin levels are associated with inflammation-related pregnancy loss following mid-trimester amniocentesis. J Matern Fetal Neonatal Med (2002) 0.75

Adverse actions are part of the job. Radiol Technol (1987) 0.75

Moral and religious influences on the amniocentesis decision. Soc Biol (1986) 0.75

Association of the X chromosomal region q11 leads to 22 and Klinefelter syndrome. Clin Genet (1981) 0.75

Letter: The origin of the hypothalamus. J Pediatr (1975) 0.75

Autosomal recessive acrocephalosyndactyly revisited. Am J Med Genet (1980) 0.75

Letter: Asynchronous growth of scalp hair in XO Turner syndrome. J Pediatr (1975) 0.75

Postintubation tracheal stenosis: diagnosis and management. S D J Med (1993) 0.75

Maternal serum alpha-fetoprotein screening: report of a pilot project in Iowa. Iowa Med (1986) 0.75

Letter: Teratogenicity of anticoagulants. J Pediatr (1975) 0.75

"Aldolase A" deficiency with syndrome of growth and developmental retardation, midfacial hypoplasia, hepatomegaly, and consanguineous parents. Birth Defects Orig Artic Ser (1977) 0.75

Outcome of alloimmunized fetuses managed solely by cordocentesis but not requiring antenatal transfusion. Fetal Diagn Ther (1994) 0.75

Chorioretinopathy and pituitary dysfunction. The CPD syndrome. Arch Ophthalmol (1981) 0.75

Clinical and biochemical correlates of a new HPRT mutation. Adv Exp Med Biol (1984) 0.75

The utility of fetal biometry as an adjunct to the multiple-marker screening test for Down syndrome. Am J Obstet Gynecol (1994) 0.75

The effect of intravascular transfusion on umbilical venous pressure in anemic fetuses with and without hydrops. Am J Obstet Gynecol (1989) 0.75

Insulin-like growth factor binding protein-3 in the detection of fetal Down syndrome pregnancies. Obstet Gynecol (1998) 0.75