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Items: 1 to 20 of 103

1.

The heterozygote advantage in phenylketonuria.

Woolf LI.

Am J Hum Genet. 1986 May;38(5):773-5. No abstract available.

3.

Phenylketonuria as a balanced polymorphism: the nature of the heterozygote advantage.

Woolf LI, McBean MS, Woolf FM, Cahalane SF.

Ann Hum Genet. 1975 May;38(4):461-9.

PMID:
1190737
4.

Frequency of phenylketonuria carriers.

Kutter D, Thoma J.

Biochem Med. 1982 Dec;28(3):285-9. No abstract available.

PMID:
7165739
5.

Heterozygote advantage for the phenylketonuria allele.

Smith I, Carter CO, Wolff OH.

J Med Genet. 1978 Jun;15(3):246-8. No abstract available.

6.

Anthropological significance of phenylketonuria and the importance of heterozygote advantage.

Saugstad LF.

Ir Med J. 1976 Sep 30;69(15):405-10. No abstract available.

PMID:
1010731
7.

On the population genetics of phenylketonuria in the G.D.R.

Machill G, Knapp A.

Hum Genet. 1976 Jan 28;31(1):107-11.

PMID:
1248817
8.

[Heterozygote identification in phenylketonuria].

Rampini S, Anders PW, Curtius HC, Marthaler T.

Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg. 1968;43(3-4):suppl 102-3. German. No abstract available.

PMID:
5761621
9.

[Frequency of phenylketonuria heterozygotes].

Kutter D.

Kinderarztl Prax. 1980 Mar;48(3):121-4. German. No abstract available.

PMID:
7392428
10.

Heterozygote advantage for the phenylketonuria allele.

Saugstad LF.

J Med Genet. 1978 Aug;15(4):317-9. No abstract available.

11.

[Method of detection of heterozygotic carrier state in phenylketonuria].

Baikov AD, Sitnichenko EI.

Lab Delo. 1973;5:293-5. Russian. No abstract available.

PMID:
4129158
12.

A role for overdominant selection in phenylketonuria? Evidence from molecular data.

Krawczak M, Zschocke J.

Hum Mutat. 2003 Apr;21(4):394-7. Review.

PMID:
12655549
13.

Mutation analysis of phenylketonuria in south Brazil.

Pérez B, Desviat LR, De Lucca M, Schmidt B, Loghin-Grosso N, Giugliani R, Pires RF, Ugarte M.

Hum Mutat. 1996;8(3):262-4. No abstract available.

PMID:
8889586
14.
15.

Carrier detection of phenylketonuria in Iranian families by variable number tandem-repeat polymorphism analysis.

Hosseini-Mazinani SM, Koochmeshgi J, Khazaee-Koohpar Z, Hosein-Pur-Nobari N, Seifati SM.

East Mediterr Health J. 2008 Nov-Dec;14(6):1445-51.

PMID:
19161120
16.

Frequency and phenotypic manifestations of schizophrenia in the parents of patients with phenylketonuria.

Kuznetsova LI.

Sov Genet. 1974 May 15;8(4):554-5. No abstract available.

PMID:
4413514
17.
18.

[Molecular genetic analysis of phenylketonuria in Bashkiria].

Viktorova TV, Murzabaeva SSh, Karunas AU, Magzhanov RV, Khusnutdinova EK.

Genetika. 1997 Jul;33(7):992-5. Russian.

PMID:
9378295
19.

The detection in the heterozygote of the metabolic effect of the recessive gene for phenylketonuria.

KNOX WE, MESSINGER EC.

Am J Hum Genet. 1958 Mar;10(1):53-60. No abstract available.

20.

[Use of modified Ayling's method for detection of homozygotes and heterozygotes for phenylketonuria gene].

Safronova EE, Rybakova NA, Annenkov GA.

Vopr Med Khim. 1982 May-Jun;28(3):70-3. Russian.

PMID:
7101818

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