Molecular studies and prenatal diagnosis of phenylketonuria in Chinese patients

Southeast Asian Journal of Tropical Medicine and Public Health

Volumn 30, Issue SUPPL. 2, 1999, Pages 63-65

  Gu, Xue Fan ^a   Liu, Xiao Qing ^a   Ye, Jun ^a   Zhang, Mei ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0347811778     PISSN: 01251562     EISSN: 26975718     Source Type: Journal    
DOI: None     Document Type: Article

References (4)

1. Chen RG. The initiation and progress of phenylketonuria programmes in China. Hong Kong Med J. 1996; 2: 282-4.
2. Wuff K, Wehnet M. Schutz M, et al. Prenatal diagnosis of phenylketonuria by haplotype analysis. Prenatal Diag 1989; 9: 421-5.
3. Gostsov A, Hisensmith RC, Naughton ER, et al. Hum Molec Gen 1993; 2: 577-81.
4. Gu XF, Zhang M, Chen RG. Phenylketonuria mutations in exon 7 of PAH gene in southern Chinese detected by denaturing gradient gel electrophoresis. J Inherit Metab Dis 1995; 18: 753-4.