{"_id":"LoDjSeXRKi7mcupGb","bibbaseid":"forest-pitfallsinprenataldiagnosisof21hydroxylasedeficiencybyamnioticfluidsteroidanalysisasixyearsexperiencein102pregnanciesatrisk-1985","author_short":["Forest, M G"],"bibdata":{"bibtype":"article","type":"article","title":"Pitfalls in prenatal diagnosis of 21-hydroxylase deficiency by amniotic fluid steroid analysis? A six years experience in 102 pregnancies at risk","volume":"458","issn":"0077-8923","shorttitle":"Pitfalls in prenatal diagnosis of 21-hydroxylase deficiency by amniotic fluid steroid analysis?","language":"eng","journal":"Annals of the New York Academy of Sciences","author":[{"propositions":[],"lastnames":["Forest"],"firstnames":["M","G"],"suffixes":[]}],"year":"1985","pmid":"3879118","keywords":"17-alpha-Hydroxyprogesterone, Adrenal Hyperplasia, Congenital, Amniotic Fluid, Androstenedione, Female, Fetal Diseases, Genetic Counseling, Histocompatibility Testing, Humans, Hydroxyprogesterones, Infant, Newborn, Karyotyping, Male, Pedigree, Pregnancy, Prenatal Diagnosis, Risk, Steroid Hydroxylases, Testosterone","pages":"130–147","author_short":["Forest, M G"],"key":"forest_pitfalls_1985","id":"forest_pitfalls_1985","bibbaseid":"forest-pitfallsinprenataldiagnosisof21hydroxylasedeficiencybyamnioticfluidsteroidanalysisasixyearsexperiencein102pregnanciesatrisk-1985","role":"author","urls":{},"keyword":["17-alpha-Hydroxyprogesterone","Adrenal Hyperplasia","Congenital","Amniotic Fluid","Androstenedione","Female","Fetal Diseases","Genetic Counseling","Histocompatibility Testing","Humans","Hydroxyprogesterones","Infant","Newborn","Karyotyping","Male","Pedigree","Pregnancy","Prenatal Diagnosis","Risk","Steroid Hydroxylases","Testosterone"],"metadata":{"authorlinks":{}},"html":""},"bibtype":"article","biburl":"https://bibbase.org/zotero/MichalRaz","dataSources":["PJeWnMTsRzaEwoJmn"],"keywords":["17-alpha-hydroxyprogesterone","adrenal hyperplasia","congenital","amniotic fluid","androstenedione","female","fetal diseases","genetic counseling","histocompatibility testing","humans","hydroxyprogesterones","infant","newborn","karyotyping","male","pedigree","pregnancy","prenatal diagnosis","risk","steroid hydroxylases","testosterone"],"search_terms":["pitfalls","prenatal","diagnosis","hydroxylase","deficiency","amniotic","fluid","steroid","analysis","six","years","experience","102","pregnancies","risk","forest"],"title":"Pitfalls in prenatal diagnosis of 21-hydroxylase deficiency by amniotic fluid steroid analysis? A six years experience in 102 pregnancies at risk","year":1985}