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Items: 10

1.

Polysome immunoprecipitation of phenylalanine hydroxylase mRNA from rat liver and cloning of its cDNA.

Robson KJ, Chandra T, MacGillivray RT, Woo SL.

Proc Natl Acad Sci U S A. 1982 Aug;79(15):4701-5.

2.

GT to AT transition at a splice donor site causes skipping of the preceding exon in phenylketonuria.

Marvit J, DiLella AG, Brayton K, Ledley FD, Robson KJ, Woo SL.

Nucleic Acids Res. 1987 Jul 24;15(14):5613-28.

3.

hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis.

Bode VC, McDonald JD, Guenet JL, Simon D.

Genetics. 1988 Feb;118(2):299-305.

4.

Collation of RFLP haplotypes at the human phenylalanine hydroxylase (PAH) locus.

Woo SL.

Am J Hum Genet. 1988 Nov;43(5):781-3. No abstract available.

5.
6.

Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and Switzerland.

Sullivan SE, Moore SD, Connor JM, King M, Cockburn F, Steinmann B, Gitzelmann R, Daiger SP, Woo SL.

Am J Hum Genet. 1989 May;44(5):652-9.

7.

Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.

Lyonnet S, Caillaud C, Rey F, Berthelon M, Frézal J, Rey J, Munnich A.

Am J Hum Genet. 1989 Apr;44(4):511-7.

8.

A cytogenetic analysis of the Punch-tudor region of chromosome 2R in Drosophila melanogaster.

O'Donnell J, Boswell R, Reynolds T, Mackay W.

Genetics. 1989 Feb;121(2):273-80.

9.

Founder effect of a prevalent phenylketonuria mutation in the Oriental population.

Wang T, Okano Y, Eisensmith RC, Harvey ML, Lo WH, Huang SZ, Zeng YT, Yuan LF, Furuyama JI, Oura T, et al.

Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2146-50.

10.

Immunological detection of phenylalanine hydroxylase protein in Drosophila melanogaster.

Silva FJ, Bel Y, Botella LM, Cotton RG, Ferré J.

Biochem J. 1992 Oct 1;287 ( Pt 1):85-9.

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