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Results: 1 to 20 of 202

1.
2.

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
[PubMed - indexed for MEDLINE]
3.

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.

PMID:
9556654
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU).

Daiger SP, Reed L, Huang SS, Zeng YT, Wang T, Lo WH, Okano Y, Hase Y, Fukuda Y, Oura T, et al.

Am J Hum Genet. 1989 Aug;45(2):319-24.

PMID:
2569272
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

[Analysis of short tandem repeats polymorphism in the phenylalanine hydroxylase gene and its application to prenatal gene diagnosis of phenylketonuria].

Huang S, Fang B, Chu H.

Zhonghua Yi Xue Za Zhi. 1995 Jan;75(1):22-4, 61. Chinese.

PMID:
7600314
[PubMed - indexed for MEDLINE]
6.
7.

A study on Chinese phenylalanine hydroxylase gene restriction site polymorphism.

Zeng YT, Huang SZ, Chen MJ, Zhang ML, Ren ZR, Xu YH, Peng SF, Woo SL.

Sci Sin B. 1988 Dec;31(12):1447-53.

PMID:
2908213
[PubMed - indexed for MEDLINE]
8.

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
[PubMed - indexed for MEDLINE]
9.

Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria families.

Svensson E, von Döbeln U, Hagenfeldt L.

Hum Genet. 1991 May;87(1):11-7.

PMID:
1674714
[PubMed - indexed for MEDLINE]
10.

A simple, rapid, and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria.

Eisensmith RC, Goltsov AA, Woo SL.

Prenat Diagn. 1994 Dec;14(12):1113-8.

PMID:
7899279
[PubMed - indexed for MEDLINE]
11.

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
[PubMed - indexed for MEDLINE]
12.

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
[PubMed - indexed for MEDLINE]
13.

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
[PubMed - indexed for MEDLINE]
14.

Modern techniques of differentiating the various phenotypes of phenylketonuria.

Guttler F.

Postgrad Med J. 1989;65 Suppl 2:S2-6.

PMID:
2576129
[PubMed - indexed for MEDLINE]
15.

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
[PubMed - indexed for MEDLINE]
16.

[Analysis of RFLP haplotypes and point mutations at the phenylalanine hydroxylase (PAH) locus in PKU families from north China].

Fang B.

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1992 Feb;14(1):46-50. Chinese.

PMID:
1350519
[PubMed - indexed for MEDLINE]
17.

[Frequencies of 6 known mutations in phenylalanine hydroxylase gene and their application in prenatal gene diagnosis].

Wang M.

Zhonghua Yi Xue Za Zhi. 1992 Nov;72(11):670-3, 702-3. Chinese.

PMID:
1338705
[PubMed - indexed for MEDLINE]
18.

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.

PMID:
2565077
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

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
[PubMed - indexed for MEDLINE]
20.

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
[PubMed - indexed for MEDLINE]

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