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Items: 1 to 20 of 209

2.
4.

RFLPs of the phenylalanine hydroxylase gene in the Italian population.

Dianzani I, Farinasso L, Fortina P, Camaschella C, Ponzone R, Dahl HH, Cotton RG, Ponzone A.

J Inherit Metab Dis. 1989;12(2):162-5.

PMID:
2569049
5.

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
6.
7.
8.

Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria.

Güttler F, Ledley FD, Lidsky AS, DiLella AG, Sullivan SE, Woo SL.

J Pediatr. 1987 Jan;110(1):68-71.

PMID:
2878985
9.

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
10.

A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria.

Goltsov AA, Eisensmith RC, Naughton ER, Jin L, Chakraborty R, Woo SL.

Hum Mol Genet. 1993 May;2(5):577-81.

PMID:
8100164
11.
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.
14.
15.

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.

16.

Haplotype analysis of the phenylalanine hydroxylase gene in Turkish phenylketonuria families.

Stuhrmann M, Riess O, Mönch E, Kurdoglu G.

Clin Genet. 1989 Aug;36(2):117-21.

PMID:
2569949
17.

Haplotype distribution at the phenylalanine hydroxylase locus in PKU families from the Moravian area of Czechoslovakia.

Kozák L, Dvoráková D, Pijácková A, Kamarýt J.

J Inherit Metab Dis. 1993;16(2):451-6.

PMID:
8105144
18.

Prenatal diagnosis of phenylketonuria by haplotype analysis.

Wulff K, Wehnert M, Schütz M, Seidlitz G, Herrmann FH.

Prenat Diagn. 1989 Jun;9(6):421-5.

PMID:
2569732
19.
20.

Haplotype analysis of phenylalanine hydroxylase alleles in polish families with phenylketonuria.

Jaruzelska J, Borski K, Riess O, Blin N, Słomski R.

Acta Biochim Pol. 1989;36(3-4):323-32.

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