The possibility for prenatal diagnosis of PKU by linkage analyses based on phenylalanine hydroxylase locus specific DNA-polymorphisms
- Author
- WOO, S. L. C1 ; ROBSON, J. H; GUTTLER, F
[1] Baylor coll. medicine, Houston TX 77007, United States - Source
Journal of inherited metabolic disease. 1984, Vol 7, Num 2, pp 139-140 ; suppl ; ref : 9 ref
- CODEN
- JIMDDP
- ISSN
- 0141-8955
- Scientific domain
- Genetics; Nutrition, obesity, metabolic disorders
- Publisher
- Springer, Dordrecht
- Publication country
- Netherlands
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aminoacidopathie Banque gène Carte physique DNA complémentaire Dépistage Enzymopathie Foetus pathologie Homme In utero Locus Maladie héréditaire Métabolisme pathologie Phenylalanine 4-monooxygenase Phénylcétonurie
- Keyword (en)
- Aminoacid disorder Gene bank Physical map Complementary DNA Screening Enzymopathy Fetal diseases Human In utero Locus Genetic disease Metabolic diseases Phenylalanine 4-monooxygenase Phenylketonuria
- Keyword (es)
- Banco genes DNA complementario Deteccion Feto patologia Enfermedad hereditaria Metabolismo patologia
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B20 Gynecology. Andrology. Obstetrics / 002B20F Pregnancy. Fetus. Placenta / 002B20F01 Management. Prenatal diagnosis
- Discipline
- Gynecology. Andrology. Obstetrics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 8984506
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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