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Journal Abstract Search

379 related items for PubMed ID: 9501609

  • 1. [Prenatal diagnosis of genetic diseases. Indications, methods, legal and ethic aspects. Neonatal screening of phenylketonuria and hypothyroidism].
    Farriaux JP.
    Rev Prat; 1997 Dec 01; 47(19):2159-68. PubMed ID: 9501609
    [No Abstract] [Full Text] [Related]

  • 2. [Prenatal and postnatal diagnosis (trisomy 21, phenylketonuria, hypothyroidism). Methods, indications, legal and ethical aspects].
    Vidailhet M.
    Rev Prat; 1994 May 01; 44(9):1241-8. PubMed ID: 7939350
    [No Abstract] [Full Text] [Related]

  • 3. [Neonatal screening for phenylketonuria and hypothyroidism].
    Maurin N, Sarles J.
    Rev Prat; 2000 Oct 01; 50(15):1728-31. PubMed ID: 11116617
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  • 4. Neonatal screening of phenylketonuria and congenital hypothyroidism in China.
    Fan GX, Jun Y, Rui-guan C.
    Southeast Asian J Trop Med Public Health; 1999 Oct 01; 30 Suppl 2():17-9. PubMed ID: 11400761
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  • 5. [Prenatal diagnosis of genetic diseases. Indications, methods, legal and ethical aspects].
    Malzac P, Mattei JF.
    Rev Prat; 2000 Oct 01; 50(15):1723-7. PubMed ID: 11116616
    [No Abstract] [Full Text] [Related]

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  • 9. Prenatal and neonatal testing and screening: a double-edged sword.
    Kenner C, Dreyer LA.
    Nurs Clin North Am; 2000 Sep 01; 35(3):627-42. PubMed ID: 10957678
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  • 10. [Problems and results of screening tests in genetic disorders].
    Knapp A.
    Z Arztl Fortbild (Jena); 1978 Jun 15; 72(11-12):535-9. PubMed ID: 676362
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  • 12. The philosophy and practice of screening for inherited diseases.
    Komrower GM.
    Pediatrics; 1974 Feb 15; 53(2):182-8. PubMed ID: 4272866
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  • 13. Screening pregnancies at risk for single gene disorders.
    Kelly TE.
    Southeast Asian J Trop Med Public Health; 1999 Feb 15; 30 Suppl 2():181-2. PubMed ID: 11400764
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  • 15. Neonatal screening for biochemical disorders.
    Holton JB.
    Br J Hosp Med; 1988 Apr 15; 39(4):317-9, 322-4. PubMed ID: 3164641
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  • 16. Newborn screening in southeastern Europe.
    Groselj U, Tansek MZ, Smon A, Angelkova N, Anton D, Baric I, Djordjevic M, Grimci L, Ivanova M, Kadam A, Kotori VM, Maksic H, Marginean O, Margineanu O, Milijanovic O, Moldovanu F, Muresan M, Murko S, Nanu M, Lampret BR, Samardzic M, Sarnavka V, Savov A, Stojiljkovic M, Suzic B, Tincheva R, Tahirovic H, Toromanovic A, Usurelu N, Battelino T.
    Mol Genet Metab; 2014 Apr 15; 113(1-2):42-5. PubMed ID: 25174966
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