المؤلفون: M. Verjaal, Nico J. Leschot, Paul F. Wiesenhaan, M. J. Becker-Bloemkolk, Jaak J. de Nef

المصدر: Human Genetics. 43:333-336

مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Prenatal diagnosis, Biology, digestive system, Encephalocele, Fingers, Pregnancy, Prenatal Diagnosis, Internal medicine, Genetics, medicine, Polycystic kidney disease, Humans, Meckel syndrome, Genetics (clinical), Polycystic Kidney Diseases, Fetus, medicine.diagnostic_test, Polydactyly, Obstetrics, Syndrome, Amniotic Fluid, medicine.disease, Endocrinology, Amniocentesis, Female, alpha-Fetoproteins

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec089e63688beede0df797c4106017d9
https://doi.org/10.1007/bf00278842