Prenatal diagnosis of type I hereditary tyrosinaemia

التفاصيل البيبلوغرافية
العنوان: Prenatal diagnosis of type I hereditary tyrosinaemia
المؤلفون: Rudolphus Berger, J.K. Ploos van Amstel, R.P.M. Jansen, M. Verjaal, I. E. T. van den Berg
المصدر: Lancet (London, England). 344(8918)
سنة النشر: 1994
مصطلحات موضوعية: Pregnancy, business.industry, DNA Mutational Analysis, Prenatal diagnosis, General Medicine, Bioinformatics, medicine.disease, Fetal Diseases, Prenatal Diagnosis, medicine, Diseases in Twins, Humans, Tyrosine, Female, Pregnancy, Multiple, business, Amino Acid Metabolism, Inborn Errors
تدمد: 0140-6736
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cecd069d8c0e9abdb3b8ad038ce61193
https://pubmed.ncbi.nlm.nih.gov/7914281
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....cecd069d8c0e9abdb3b8ad038ce61193
قاعدة البيانات: OpenAIRE