Published in Pediatrics on February 01, 1981
Birth defects following maternal exposure to ergotamine, beta blockers, and caffeine. J Med Genet (1988) 1.46
Hemifacial microsomia: from gestation to childhood. J Craniofac Surg (2009) 1.02
Reproduction abnormalities and twin pregnancies in parents of sporadic patients with oculo-auriculo-vertebral spectrum/Goldenhar syndrome. Hum Genet (2007) 1.00
The surviving monozygotic twin. Arch Dis Child (1986) 0.91
Atresia of the ascending colon: a rarity. APSP J Case Rep (2010) 0.85
Congenital anomalies in multiple births after early loss of a conceptus. Hum Reprod (2008) 0.80
Vasoactive exposures during pregnancy and risk of microtia. Birth Defects Res A Clin Mol Teratol (2012) 0.78
Neurovascular developmental interaction: a specific form of vascular maldevelopment in the malformed brain. I. An experimental study and proposal of a new teratological concept. Childs Nerv Syst (1996) 0.77
Recognition of the fetal alcohol syndrome in early infancy. Lancet (1973) 8.57
Pattern of malformation in offspring of chronic alcoholic mothers. Lancet (1973) 7.45
Birth outcomes in pregnant women taking fluoxetine. N Engl J Med (1996) 5.38
Older paternal age and fresh gene mutation: data on additional disorders. J Pediatr (1975) 2.97
Liver in Felty's syndrome. Br Med J (1970) 2.75
Relationships of upper gastrointestinal motor and sensory function with glycemic control. Diabetes Care (2001) 2.60
Sarafotoxin S6c: an agonist which distinguishes between endothelin receptor subtypes. Biochem Biophys Res Commun (1991) 2.54
Massively parallel 454 sequencing indicates hyperdiverse fungal communities in temperate Quercus macrocarpa phyllosphere. New Phytol (2009) 2.53
The amniotic band disruption complex: timing of amniotic rupture and variable spectra of consequent defects. J Pediatr (1979) 2.46
Epidemiology of fetal alcohol syndrome in a South African community in the Western Cape Province. Am J Public Health (2000) 2.30
Outcome in offspring of chronic alcoholic women. Lancet (1974) 2.27
Clinical and molecular diagnosis of Miller-Dieker syndrome. Am J Hum Genet (1991) 2.09
Do we need the term "FAE"? Pediatrics (1995) 2.08
Neuropsychological comparison of alcohol-exposed children with or without physical features of fetal alcohol syndrome. Neuropsychology (1998) 2.03
Heavy prenatal alcohol exposure with or without physical features of fetal alcohol syndrome leads to IQ deficits. J Pediatr (1997) 2.02
The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly. Hum Mol Genet (1999) 2.00
Prenatal cocaine exposure and fetal vascular disruption. Pediatrics (1990) 1.97
Type 2 diabetes mellitus in minority children and adolescents. An emerging problem. Endocrinol Metab Clin North Am (1999) 1.77
Gastric emptying in diabetes: clinical significance and treatment. Diabet Med (2002) 1.75
Natural history of diabetic gastroparesis. Diabetes Care (1999) 1.74
The fetal alcohol syndrome. Teratology (1975) 1.70
Abnormalities of the corpus callosum in children prenatally exposed to alcohol. Alcohol Clin Exp Res (1995) 1.67
A decrease in the size of the basal ganglia in children with fetal alcohol syndrome. Alcohol Clin Exp Res (1996) 1.67
Vascular steal: the pathogenetic mechanism producing sirenomelia and associated defects of the viscera and soft tissues. Pediatrics (1986) 1.60
Potentially modifiable risk factors for adverse pregnancy outcomes in women with psoriasis. Br J Dermatol (2010) 1.57
The vascular pathogenesis of gastroschisis: intrauterine interruption of the omphalomesenteric artery. J Pediatr (1981) 1.56
Limb/pelvis hypoplasia/aplasia with skull defect (Schinzel phocomelia): distinctive features and prenatal detection. Am J Med Genet (2001) 1.55
Possible common pathogenetic mechanisms for Poland sequence and Adams-Oliver syndrome. Am J Med Genet (1991) 1.54
Ovarian dysgenesis in individuals with chromosomal abnormalities. Hum Genet (1991) 1.53
The Williams elfin facies syndrome. A new perspective. J Pediatr (1975) 1.50
Update on new developments in the study of human teratogens. Teratology (2002) 1.49
Laterality defects in conjoined twins: implications for normal asymmetry in human embryogenesis. Am J Med Genet (1988) 1.49
Central nervous system anomalies associated with meningomyelocele, hydrocephalus, and the Arnold-Chiari malformation: reappraisal of theories regarding the pathogenesis of posterior neural tube closure defects. Neurosurgery (1986) 1.48
Seasonally dynamic fungal communities in the Quercus macrocarpa phyllosphere differ between urban and nonurban environments. New Phytol (2010) 1.45
Abnormal development of the cerebellar vermis in children prenatally exposed to alcohol: size reduction in lobules I-V. Alcohol Clin Exp Res (1996) 1.45
A syndrome of methylmalonic aciduria, homocystinuria, megaloblastic anemia and neurologic abnormalities in a vitamin B12-deficient breast-fed infant of a strict vegetarian. N Engl J Med (1978) 1.42
Fetal alcohol syndrome. Experience with 41 patients. JAMA (1976) 1.39
Delineation of the Costello syndrome. Am J Med Genet (1991) 1.39
Sudden death in Williams syndrome: report of ten cases. J Pediatr (1996) 1.38
Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1. Nat Genet (1993) 1.37
Isolated hemihyperplasia (hemihypertrophy): report of a prospective multicenter study of the incidence of neoplasia and review. Am J Med Genet (1998) 1.34
Prader-Willi and Angelman syndromes: diagnosis with a bisulfite-treated methylation-specific PCR method. Am J Med Genet (1997) 1.34
Prophylactic activity of tetracycline against Brugia pahangi infection in jirds (Meriones unguiculatus). J Parasitol (1993) 1.33
Verbal learning and memory in children with fetal alcohol syndrome. Alcohol Clin Exp Res (1996) 1.33
Seed Dormancy in Red Rice : VII. Structure-Activity Studies of Germination Stimulants. Plant Physiol (1989) 1.32
The sequence of RNA segment 1 of influenza virus A/NT/60/68 and its comparison with the corresponding segment of strains A/PR/8/34 and A/WSN/33. Nucleic Acids Res (1983) 1.28
Human brain fibroblast growth factor. Isolation and partial chemical characterization. FEBS Lett (1985) 1.27
Congenital skin defects and fetus papyraceus. J Pediatr (1977) 1.26
Localization and binding of transforming growth factor-beta isoforms in mouse preimplantation embryos and in delayed and activated blastocysts. Dev Biol (1992) 1.26
Apnea and sudden unexpected death in infants with achondroplasia. J Pediatr (1984) 1.26
The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutations. Clin Genet (2004) 1.25
Natural history of the fetal alcohol syndrome: a 10-year follow-up of eleven patients. Lancet (1985) 1.25
A new syndrome of mental deficiency with craniofacial, limb, and anal abnormalities. J Pediatr (1976) 1.24
Prenatal alcohol exposure alters the patterns of facial asymmetry. Alcohol (2010) 1.21
Breech presentation as an indicator of fetal abnormality. J Pediatr (1975) 1.21
Gastric emptying in diabetes: an overview. Diabet Med (1996) 1.20
Two forms of cutis laxa presenting in the newborn period. Acta Paediatr Scand (1978) 1.20
Mirror hands and feet with a distinct nasal defect, an autosomal dominant condition. Am J Med Genet (1993) 1.19
Unexplained acute backache in longstanding ankylosing spondylitis. Br Med J (Clin Res Ed) (1985) 1.16
Gastroschisis: abdominal wall disruption secondary to early gestational interruption of the omphalomesenteric artery. Semin Perinatol (1983) 1.16
Purification of a growth factor for ovarian cells from bovine pituitary glands. Proc Natl Acad Sci U S A (1974) 1.14
Brachmann-de Lange syndrome: evidence for autosomal dominant inheritance. Am J Med Genet (1985) 1.14
Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster. Am J Hum Genet (1999) 1.13
Effects of age on concentrations of plasma cholecystokinin, glucagon-like peptide 1, and peptide YY and their relation to appetite and pyloric motility. Am J Clin Nutr (1999) 1.12
A second patient with partial deletion of the short arm of chromosome 3: karyotype 46,XY,del(3)(p25). J Med Genet (1982) 1.12
The MIller-Dieker syndrome. Pediatrics (1980) 1.11
Craniosynostosis--radial aplasia syndrome. J Pediatr (1974) 1.11
Identification of a thymidylate synthase ribonucleoprotein complex in human colon cancer cells. Mol Cell Biol (1994) 1.11
Gastroparesis: prevalence, clinical significance and treatment. Can J Gastroenterol (2001) 1.10
Influenza A virus evolution: complete sequences of influenza A/NT/60/68 RNA segment 3 and its predicted acidic P polypeptide compared with those of influenza A/PR/8/34. Virology (1982) 1.09
Lymphedema in Noonan syndrome: clues to pathogenesis and prenatal diagnosis and review of the literature. Am J Med Genet (1987) 1.09
Can prenatal ultrasound detect the effects of in-utero alcohol exposure? A pilot study. Ultrasound Obstet Gynecol (2009) 1.09
New autosomal dominant branchio-oculo-facial syndrome. Am J Med Genet (1987) 1.08
Missense mutation serine106----proline causes 17 alpha-hydroxylase deficiency. J Biol Chem (1991) 1.08
The Bannayan syndrome: an autosomal dominant disorder consisting of macrocephaly, lipomas, hemangiomas, and risk for intracranial tumors. Pediatrics (1982) 1.07
Immediate chromosome diagnosis on bone marrow cells: an aid to management of the malformed newborn infant. J Pediatr (1979) 1.07
High variability and disomic segregation of microsatellites in the octoploid Fragaria virginiana Mill. (Rosaceae). Theor Appl Genet (2003) 1.06
A decrease in the size of the basal ganglia following prenatal alcohol exposure: a preliminary report. Neurotoxicol Teratol (1994) 1.05
Fetal alcohol syndrome: a case report of neuropsychological, MRI and EEG assessment of two children. Alcohol Clin Exp Res (1992) 1.05
Scintigraphic measurement of gastric emptying and ultrasonographic assessment of antral area: relation to appetite. Gut (1996) 1.05
Monozygotic twins discordant for the Russell-Silver syndrome. Am J Med Genet (1995) 1.05
Patterns of malformation in children with congenital diaphragmatic defects. J Pediatr (1990) 1.05
Automated diagnosis of fetal alcohol syndrome using 3D facial image analysis. Orthod Craniofac Res (2008) 1.04
Gastric emptying of a liquid nutrient meal in the critically ill: relationship between scintigraphic and carbon breath test measurement. Gut (2011) 1.04
The umbilical cord twist: origin, direction, and relevance. Am J Obstet Gynecol (1987) 1.03
Thymidylate synthase binds to c-myc RNA in human colon cancer cells and in vitro. Mol Cell Biol (1995) 1.02
Congenital scalp defects and vitreoretinal degeneration: redefining the Knobloch syndrome. Am J Med Genet (1993) 1.02
Compression-related defects from early amnion rupture: evidence for mechanical teratogenesis. J Pediatr (1981) 1.01
Vascular pathogenesis of transverse limb reduction defects. J Pediatr (1982) 1.01
Synovial fluid macrophages and blood monocytes differ in their response to IL-4. J Immunol (1993) 1.00
Pregnancy outcome in women exposed to leflunomide before or during pregnancy. Arthritis Rheum (2012) 1.00
Toluene embryopathy: delineation of the phenotype and comparison with fetal alcohol syndrome. Pediatrics (1994) 0.99
The effect of reducing reagents on binding of thymidylate synthase protein to thymidylate synthase messenger RNA. J Biol Chem (1994) 0.98
Extension of the cleft lip phenotype: the subepithelial cleft. Am J Med Genet (1993) 0.96