about
Developmental neurotoxicity assessments: selecting exposure parametersCross-regulatory interactions between Fgf8 and Shh in the avian frontonasal prominenceErythropoietin contributes to implantation: ectopic hemoglobin synthesis in decidual cells of miceEFNB1 mutation at the ephrin ligand-receptor dimerization interface in a patient with craniofrontonasal syndrome.Novel alternative splicing of human faciogenital dysplasia 1 gene.Historical control data on prenatal developmental toxicity studies in rabbits.Historical control data on reproductive abilities and incidences of spontaneous fetal malformations in Wistar Hannover GALAS rats.Historical control data on developmental toxicity studies in rodents.The dopaminergic system in attention deficit/hyperactivity disorder.Virtual bronchoscopy through the fetal airways in a case of cervical teratoma using magnetic resonance imaging data.Analysis of fetal DNA from maternal peripheral blood by lectin-polymerase chain reaction-single strand conformation polymorphism.Studies on protocadherin-2 expression in the human fetal central nervous system.Prevalence of congenital limb defects: Data from birth defects registries in three provinces in Southern Thailand.Cleft lip and palate in mice treated with 2,3,7,8-tetrachlorodibenzo-p-dioxin: a morphological in vivo study.Comments from the Developmental Neurotoxicology Committee of the Japanese Teratology Society on the OECD Guideline for the Testing of Chemicals, Proposal for a New Guideline 426, Developmental Neurotoxicity Study, Draft Document (October 2006 versioMorphometric study on the characteristic external features of normal and abnormal human embryos.Fetal cytomegalovirus infection manifesting as transient pancytopenia.Effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin suggests abnormal palate development after palatal fusion.New method for detecting antiandrogenic effects through the measurement of external genitalia in rabbits.Early onset of fatty liver in growth-restricted rat fetuses and newborns.Neuroanatomic and magnetic resonance imaging references for normal development of cerebral sulci of laboratory primate, cynomolgus monkeys (Macaca fascicularis).Digitization of clinical and epidemiological data from the Kyoto Collection of Human Embryos: maternal risk factors and embryonic malformations.Down syndrome and personalized medicine: changing paradigms from genotype to phenotype to treatment.Population-based case-control study of oral ketoconazole treatment for birth outcomes.Blastopathies and microcephaly in a Chornobyl impacted region of Ukraine.Abnormal giant cells in the cerebral lesions of tuberous sclerosis complex.Isolated levocardia: prenatal diagnosis and management.Hyperthermia in utero due to maternal influenza is an environmental risk factor for schizophrenia.Necessity to establish new risk assessment and risk communication for human fetal exposure to multiple endocrine disruptors in Japan.Developmental toxicity of estrogenic chemicals on rodents and other species.Endocrine disruptor issues in Japan.Architectural changes in the developing human brain based on the matrix cell theory.Analysis of genitourinary anomalies in patients with VACTERL (Vertebral anomalies, Anal atresia, Cardiac malformations, Tracheo-Esophageal fistula, Renal anomalies, Limb abnormalities) association.Antiandrogenic effects of dibutyl phthalate and its metabolite, monobutyl phthalate, in rats.The interplay of genetic and environmental factors in craniofacial morphogenesis: holoprosencephaly and the role of cholesterol.Molecular pathology of human cerebral malformations.Fukuyama-type congenital muscular dystrophy (FCMD) and alpha-dystroglycanopathy.Brain slice culture for analysis of developmental brain disorders with special reference to congenital cytomegalovirus infection.Zebrafish as a novel experimental model for developmental toxicology.A genetic mouse model carrying the nonfunctional xeroderma pigmentosum group G gene.
P1433
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P1433
description
journal
@en
revista científica
@es
rivista scientifica
@it
wetenschappelijk tijdschrift van John Wiley & Sons
@nl
wissenschaftliche Fachzeitschrift
@de
name
Congenital anomalies
@en
Congenital anomalies
@es
Congenital anomalies
@it
Congenital anomalies
@nl
type
label
Congenital anomalies
@en
Congenital anomalies
@es
Congenital anomalies
@it
Congenital anomalies
@nl
prefLabel
Congenital anomalies
@en
Congenital anomalies
@es
Congenital anomalies
@it
Congenital anomalies
@nl
P31
P243
P3181
P356
P1055
P1156
P123
P1250
P1277
P1476
Congenital anomaliesen
@und
P236
P243
P3181
P356
10.1111/(ISSN)1741-4520