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Items: 1 to 20 of 103

1.

Linkage analysis using heterozygote detection in phenylketonuria.

Paul TD, Brandt IK, Elsas LJ, Jackson CE, Nance CS, Nance WE.

Clin Genet. 1979 Oct;16(4):217-32.

PMID:
519892
2.

Phenylketonuria heterozygote detection in families with affected children.

Paul TD, Brandt IK, Elsas LJ, Jackson CE, Mamunes P, Nance CS, Nance WE.

Am J Hum Genet. 1978 May;30(3):293-301.

3.

Improved identification of heterozygotes for phenylketonuria using blood neopterin and biopterin.

Alós T, Bel Y, Cabello ML, Catalá JL, Dalmau J, Ferré J, García AM, Ruiz-Vázquez P.

J Inherit Metab Dis. 1993;16(2):457-64.

PMID:
8412006
4.

Plasma phenylalanine, tyrosine, and tryptophan in schizophrenia.

Potkin SG, Cannon-Spoor HE, DeLisi LE, Neckers LM, Wyatt RJ.

Arch Gen Psychiatry. 1983 Jul;40(7):749-52.

PMID:
6860076
6.

Classic phenylketonuria: diagnosis through heterozygote detection.

Griffin RF, Elsas LJ.

J Pediatr. 1975 Apr;86(4):512-7.

PMID:
1127497
7.
9.

Heterozygote detection in phenylketonuria.

Güttler F, Hansen G.

Clin Genet. 1977 Feb;11(2):137-46.

PMID:
837563
13.

Relative reliability of three different discriminant analysis methods for detecting PKU gene carriers.

Wenger SL, Vieira PW, Breck JM, Steele MW.

Clin Genet. 1986 Jul;30(1):38-40.

PMID:
3757295
14.
15.
16.

Discrimination of heterozygotes for phenylketonuria, persistent hyperphenylalaninemia and controls by phenylalanine loading.

Blitzer MG, Bailey-Wilson JE, Shapira E.

Clin Chim Acta. 1986 Dec 30;161(3):347-52. No abstract available.

PMID:
3802540
18.
19.

Evaluation of an aspartame loading test for the detection of heterozygotes for classical phenylketonuria.

Silva LC, Pires RF, Coelho JC, Jardim LB, Giugliani R.

Clin Genet. 1997 Apr;51(4):231-5.

PMID:
9184243
20.

[A study of phenylketonuria heterozygotes screening in married population of Tianjin area].

Song L, Xu F, Meng Y, Wang X, Liu C, Gao W, Shan Z, Liu C, Ding Z.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2001 Feb;18(1):56-8. Chinese.

PMID:
11172645

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