• An epidemiologic study of environmental and genetic factors in congenital hydrocephalus
• Anomalies in thyroid function in children with trisomy 21
• Anomalies of thyroid function in children with Down syndrome
• Are some multiple congenital anomalies with mental retardation (MCA/MR) the clinical expression of rare autosomal fragile sites?
• Associated anomalies in anophthalmia and microphthalmia
• Associated anomalies in cases with achondroplasia
• Associated anomalies in cases with anorectal anomalies
• Associated anomalies in cases with esophageal atresia
• ASSOCIATED ANOMALIES IN CASES WITH LIMB REDUCTION DEFICIENCIES
• Associated congenital anomalies among cases with Down syndrome
• Associated malformations among infants with anophthalmia and microphthalmia
• Associated malformations among infants with radial ray deficiency
• Associated malformations in cases with congenital diaphragmatic hernia
• Associated malformations in patients with anorectal anomalies
• Associated malformations in patients with esophageal atresia
• Associated malformations in patients with limb reduction deficiencies
• ASSOCIATED NON DIAPHRAGMATIC ANOMALIES AMONG CASES WITH CONGENITAL DIAPHRAGMATIC HERNIA
• Associated noncardiac congenital anomalies among cases with congenital heart defects
• Associated nonurinary congenital anomalies among infants with congenital anomalies of kidney and urinary tract (CAKUT)
• Association of Duane anomaly with mental retardation, cardiac and urinary tract abnormalities: a new autosomal recessive condition?
• Epidemiology of Down syndrome in 118,265 consecutive births
• Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examination
• Evaluation of routine prenatal diagnosis by a registry of congenital anomalies
• Evaluation of routine prenatal ultrasound examination in detecting fetal chromosomal abnormalities in a low risk population
• Impact of prenatal diagnosis on livebirth prevalence of children with congenital anomalies
• Impact of routine fetal ultrasonographic screening on the prevalence of Down syndrome in non aged mothers
• Lymphedema combined with brachydactyly and tachycardia
• Maternal trace elements, vitamin B12, vitamin A, folic acid, and fetal malformations
• Mental retardation, ataxia, seizures, dysmorphia, and hydrocephaly in two sibs. Angelman syndrome or new syndrome
• No evidence for genomic imprinting in liveborn Down syndrome patients
• No evidence for genomic imprinting in liver-born Down syndrome patients
• Oligodontia, microcephaly and facial dysmorphia syndrome
• Omphalocele and gastroschisis and associated malformations
• Recent trends in the prevalence of Down syndrome in north-eastern France
• Rett-like syndrome in fragile X syndrome
• Risk factors in congenital abdominal wall defects (omphalocele and gastroschisi): a study in a series of 265,858 consecutive births
• Risk factors in congenital anal atresias
• Risk factors in congenital heart disease
• Risk factors in internal urinary system malformations
• Study of 156 cases of polyhydramnios and congenital malformations in a series of 118,265 consecutive births
• Study of 224 cases of oligohydramnios and congenital malformations in a series of 225,669 consecutive births
• Study of 290 cases of polyhydramnios and congenital malformations in a series of 225,669 consecutive births
• Study of Down syndrome in 238,942 consecutive births
• Ventricular extrasystoles with syncopal episodes, perodactyly, and Robin in sequence in three generations: a new inherited MCA syndrome?