• A case-control etiologic study of microcephaly
• A family study of cases with unidentified multiple congenital abnormality
• A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3
• A morphological and family study on isolated terminal transverse type of congenital limb deficiency in Hungary, 1975-1984
• A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13
• A nationwide evaluation of multiple congenital abnormalities in Hungary
• A new case of neonatal progeroid syndrome with agenesis of corpus callosum
• A new heart defect-brachydactyly syndrome
• A pathogenesis-oriented classification of congenital abnormalities
• A plea from so-called "Eastern-Europe"
• A population-based case-control teratologic study of acetylsalicylic acid treatments during pregnancy
• A population-based case-control teratologic study of ampicillin treatment during pregnancy
• A population-based case-control teratologic study of oral dipyrone treatment during pregnancy
• A population-based case-control teratologic study of promethazine use during pregnancy
• A Possible Association between Oral Aminophylline Treatment during Pregnancy and Skeletal Congenital Abnormalities
• A study of the effects of large doses of glutethimide that were used for self-poisoning during pregnancy on human fetuses
• A study of the teratogenic and fetotoxic effects of large doses of chlordiazepoxide used for self-poisoning by 35 pregnant women
• Acute respiratory infections during pregnancy and congenital abnormalities: a population-based case-control study
• ADAM "sequence" part II: hypothesis and speculation
• An aetiological study on 6 to 14 years-old children with severe visual handicap in Hungary
• Association of AXIN2 with non-syndromic oral clefts in multiple populations
• Association of certain chronic maternal diseases with the risk of specific congenital heart defects: a population-based study
• Association of drug treatments in pregnant women with the risk of external ear congenital abnormalities in their offspring: a population-based case-control study
• Association of Shokeir syndrome (congenital universal alopecia, epilepsy, mental subnormality and pyorrhea) and giant pigmented nevus
• Autosomal recessive acrorenal syndrome
• Birth outcomes of cases with left-sided obstructive defects of the heart in the function of maternal socio-demographic factors: a population-based case-control study
• Birth outcomes of cases with unclassified multiple congenital abnormalities and pregnancy complications in their mothers depending on the number of component defects. Population-based case-control study
• Birth prevalence of Poland sequence and proportion of its familial cases
• Birth prevalence study of the Apert syndrome
• Birth weight and congenital anomalies following poisonous mushroom intoxication during pregnancy
• Cockayne syndrome type III with high intelligence
• Congenital abnormalities and indicators of germinal mutations in the vicinity of an acrylonitrile producing factory
• Congenital abnormalities and indicators of germinal mutations in the vicinity of the Paks nuclear plant, Hungary
• Congenital abnormalities associated with limb deficiency defects: a population study based on cases from the Hungarian Congenital Malformation Registry (1975-1984)
• Dandy-Walker malformation and polydactyly: a possible expression of hydrolethalus syndrome
• Delineation of a multiple congenital abnormality syndrome in the offspring of pregnant women affected with high fever-related disorders: a population-based study
• Description and mission evaluation of the Hungarian case-control surveillance of congenital abnormalities, 1980-1996
• Disruption of the PDGFB gene in a 1;22 translocation patient does not cause Costello syndrome
• Distribution of associated component abnormalities in cases with unclassified multiple ("syndromic") anota/microtia
• Distribution of maternal age and birth order groups in cases with unclassified multiple congenital abnormalities according to the number of component abnormalities: a national population-based case-control study
• Environmental trichlorfon and cluster of congenital abnormalities
• Evaluation of drug intake during pregnancy in the Hungarian Case-Control Surveillance of Congenital Anomalies
• Familial combination of brachydactyly, type E and atrial septal defect, type II
• Fetal varicella syndrome
• Genetic counseling in a case of Takayasu arteritis
• Gollop-Wolfgang complex: tibial hemimelia associated with bifid femur and hypodactyly
• Holt-Oram syndrome
• Human germinal mutagenic effects in relation to intentional and accidental exposure to toxic agents
• Hungarian case with Costello syndrome and translocation t(1,22)
• Hungarian surveillance of germinal mutations. Lack of detectable increase in indicator conditions caused by germinal mutations following the Chernobyl accident
• Incidence of legal abortions and congenital abnormalities in Hungary
• Increasing total prevalence rate of cases with Down syndrome in Hungary
• International Commission for Protection against Environmental Mutagens and Carcinogens. ICPEMC Working Paper No. 10. A new approach to germinal mutation surveillance: pair-wise evaluation of component elements in unidentified multiple congenital abnormali
• IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families
• Isolated hypospadias in 5 brothers
• IVIC syndrome report by Czeizel et al
• IVIC syndrome: report of a third family
• Kallmann syndrome in three unrelated women and an association with femur-fibula-ulna dysostosis in one case
• Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritance
• Maternal risk factors in the origin of isolated hypospadias: a population-based case-control study
• Maternal severe migraine and risk of congenital limb deficiencies
• Maternal use of nutritional supplements during the first month of pregnancy and decreased risk of Down's syndrome: case-control study
• Microcephaly, microphthalmia, congenital cataract, with calcification of the basal ganglia: MCA/MR syndrome
• Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome
• Multiple synostosis
• Nitrofurantoin and congenital abnormalities
• No association of maternal vitamin E intake with higher risk of cardiovascular malformations in children: a population-based case-control study
• Oral clefts with associated anomalies: findings in the Hungarian Congenital Abnormality Registry
• Oral clefts with associated anomalies: methodological issues
• Pathogenesis of severe vision deficiency in school-age children in Hungary
• Patterns of acrorenal malformation associations
• Population surveillance of sentinel anomalies
• Population-based case-control study of the common cold during pregnancy and congenital abnormalities
• Prevention of congenital abnormalities by periconceptional multivitamin supplementation
• Public health aspects of the Martin-Bell syndrome
• Refinement and delineation of the breakpoint regions of a chromosome 1;22 translocation in a patient with Costello syndrome
• Risk and benefit of drug use during pregnancy
• Risk factors in the origin of congenital left-ventricular outflow-tract obstruction defects of the heart: a population-based case-control study
• Scope of Alagille syndrome
• Senna treatment in pregnant women and congenital abnormalities in their offspring--a population-based case-control study
• Short-Term Oral Diazepam Treatment during Pregnancy : A Population-Based Teratological Case-Control Study
• Six cases of basal cell nevus carcinoma in three families
• Smoking during pregnancy and Poland sequence: results of a population-based registry and a case-control registry
• Split hand/split foot, syndactyly, urinary tract obstruction, radial, diaphragmatic, and neural tube defects: Czeizel-Losonci syndrome?
• Study of isolated apparent amniogenic limb deficiency in Hungary, 1975-1984
• Syndrome of cataract, mild microcephaly, mental retardation and Perthes-like changes in sibs
• Syndromes, disorders and maternal risk factors associated with neural tube defects (VII)
• Teratogenic effect of hydroxyethylrutoside, a flavonoid derivate drug--a population-based case-control study
• Teratologic evaluation of 178 infants born to mothers who attempted suicide by drugs during pregnancy
• The deltaccr5 mutation conferring protection against HIV-1 in Caucasian populations has a single and recent origin in Northeastern Europe
• The ethical issues of the postmarketing surveillance of drug teratogenicity in Hungary
• The evaluation of the germinal mutagenic impact of Chernobyl radiological contamination in Hungary
• The first case of a child born with fetal valproic acid syndrome in Hungary
• The importance of molecular genetic diagnosis of Martin-Bell disease in genetic counseling
• The load of genetic and partially genetic disease in man. IV. Severe visual handicaps and profound childhood deafness in Hungarian school-age children
• The second report of Knobloch syndrome
• The spectrum of congenital anomalies of the VATER association: an international study
• Therapeutic importance of the diagnosis of Kallmann syndrome
• Use of cephalosporins during pregnancy and in the presence of congenital abnormalities: a population-based, case-control study
• Using the Hungarian Birth Defects Registry for surveillance, research and intervention