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Items: 14

1.

Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria.

Lidsky AS, Ledley FD, DiLella AG, Kwok SC, Daiger SP, Robson KJ, Woo SL.

Am J Hum Genet. 1985 Jul;37(4):619-34.

2.

Phenylketonuria and other phenylalanine hydroxylation mutants in man.

Scriver CR, Clow CL.

Annu Rev Genet. 1980;14:179-202. Review. No abstract available.

PMID:
7011173
3.

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.

4.

The PKU locus in man is on chromosome 12.

Lidksy AS, Robson KJ, Thirumalachary C, Barker PE, Ruddle FH, Woo SL.

Am J Hum Genet. 1984 May;36(3):527-33.

5.

Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria.

Woo SL, Lidsky AS, Güttler F, Chandra T, Robson KJ.

Nature. 1983 Nov 10-16;306(5939):151-5.

PMID:
6316140
6.

Gene transfer and expression of human phenylalanine hydroxylase.

Ledley FD, Grenett HE, DiLella AG, Kwok SC, Woo SL.

Science. 1985 Apr 5;228(4695):77-9.

PMID:
3856322
7.

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.

8.
9.

Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria.

DiLella AG, Marvit J, Lidsky AS, Güttler F, Woo SL.

Nature. 1986 Aug 28-Sep 3;322(6082):799-803.

PMID:
3018584
10.

Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase.

Kwok SC, Ledley FD, DiLella AG, Robson KJ, Woo SL.

Biochemistry. 1985 Jan 29;24(3):556-61.

PMID:
2986678
11.

An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2.

DiLella AG, Marvit J, Brayton K, Woo SL.

Nature. 1987 May 28-Jun 3;327(6120):333-6.

PMID:
2884570
12.

Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria.

Chakraborty R, Lidsky AS, Daiger SP, Güttler F, Sullivan S, Dilella AG, Woo SL.

Hum Genet. 1987 May;76(1):40-6.

PMID:
2883110
13.

Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus in prenatal diagnosis of phenylketonuria.

Daiger SP, Lidsky AS, Chakraborty R, Koch R, Güttler F, Woo SL.

Lancet. 1986 Feb 1;1(8475):229-32.

PMID:
2868252
14.

Prenatal diagnosis of classic phenylketonuria by DNA analysis.

Lidsky AS, Güttler F, Woo SL.

Lancet. 1985 Mar 9;1(8428):549-51.

PMID:
2857902

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