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Results: 1 to 20 of 103

Similar articles for PubMed (Select 6700105)

1.

Prenatal diagnosis of classical phenylketonuria by gene mapping.

Woo SL, Lidsky AS, Güttler F, Thirumalachary C, Robson KJ.

JAMA. 1984 Apr 20;251(15):1998-2002. No abstract available.

PMID:
6700105
2.

Prenatal diagnosis and carrier detection of classic phenylketonuria by gene analysis.

Woo SL.

Pediatrics. 1984 Sep;74(3):412-23. No abstract available.

PMID:
6472974
3.

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
4.

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.

5.

[Genetic diagnosis in classical phenylketonuria].

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

Z Arztl Fortbild (Jena). 1988;82(22):1127-31. German. No abstract available.

PMID:
2907835
6.

[Phenylketonuria].

Oura T.

Tanpakushitsu Kakusan Koso. 1988 Apr;33(5):487-92. Japanese. No abstract available.

PMID:
2908394
7.

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
8.

[Genetic heterogeneity and approaches to the prenatal diagnosis of phenylketonuria (review)].

Chestkov VV, Shishkin SS.

Vopr Med Khim. 1986 Jul-Aug;32(4):7-12. Review. Russian.

PMID:
3020793
9.

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
10.

Recombinant DNA probes used to detect genetic disorders of the liver.

Kidd VJ, Woo SL.

Hepatology. 1984 Jul-Aug;4(4):731-6. Review. No abstract available.

PMID:
6086486
11.

[Antenatal gene diagnosis of phenylketonuria].

Zeng YT.

Zhonghua Yi Xue Za Zhi. 1986 Aug;66(8):493-4. Chinese. No abstract available.

PMID:
3096539
12.

Molecular biology of phenylketonuria.

Güttler F, DiLella AG, Ledley FD, Lidsky AS, Kvok SC, Marvit J, Woo SL.

Eur J Pediatr. 1987;146 Suppl 1:A5-11. No abstract available.

PMID:
2891509
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
15.

The human phenylalanine hydroxylase gene.

Woo SL, Güttler F, Ledley FD, Lidsky AS, Kwok SC, DiLella AG, Robson KJ.

Prog Clin Biol Res. 1985;177:123-35. No abstract available.

PMID:
2989834
16.

Detection of point mutations of the phenylalanine hydroxylase gene and prenatal diagnosis of phenylketonuria.

Fang B, Yuan L, Wang M, Huang S, Wang T, Miao S, Ye J, Sun N, Lo H, Savio LC.

Chin Med Sci J. 1992 Dec;7(4):205-8.

PMID:
1307495
17.
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19.

Phenylalanine hydroxylase expression in liver of a fetus with phenylketonuria.

Ledley FD, Koch R, Jew K, Beaudet A, O'Brien WE, Bartos DP, Woo SL.

J Pediatr. 1988 Sep;113(3):463-8.

PMID:
2900886
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