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Items: 1 to 20 of 24

1.

Phenylketonuria (PKU) and the single gene: an old story retold.

Murphey RM.

Behav Genet. 1983 Mar;13(2):141-57. No abstract available.

PMID:
6860251
2.

Neurological aspects of adult phenylketonuria.

Pietz J.

Curr Opin Neurol. 1998 Dec;11(6):679-88. Review.

PMID:
9870137
3.

An appraisal of the application of recombinant DNA techniques to chromosome defects.

Ellis KP, Davies KE.

Biochem J. 1985 Feb 15;226(1):1-11. Review. No abstract available.

4.

[Advances in the studies of molecular heredity of phenylketonuria].

Zhang Z, He YS.

Yi Chuan. 2004 Sep;26(5):729-34. Review. Chinese.

PMID:
15640093
5.

What we know that could influence future treatment of phenylketonuria.

Sarkissian CN, Gámez A, Scriver CR.

J Inherit Metab Dis. 2009 Feb;32(1):3-9. doi: 10.1007/s10545-008-0917-7. Epub 2008 Aug 3. Review.

PMID:
18668342
6.

The PAH gene, phenylketonuria, and a paradigm shift.

Scriver CR.

Hum Mutat. 2007 Sep;28(9):831-45. Review.

PMID:
17443661
7.

[Mapping of the human genome by gene dosage method].

Głogowska I.

Pol Tyg Lek. 1985 Mar 4;40(9):273-7. Review. Polish. No abstract available.

PMID:
3889888
8.
9.
10.

Genes and inheritance.

Middelton LA, Peters KF, Helmbold EA.

Cancer Nurs. 1997 Apr;20(2):129-47; quiz 148-51. Review.

PMID:
9145562
11.

Population genetics of phenylketonuria.

Eisensmith RC, Woo SL.

Acta Paediatr Suppl. 1994 Dec;407:19-26. Review.

PMID:
7766949
12.

The structural basis of phenylketonuria.

Erlandsen H, Stevens RC.

Mol Genet Metab. 1999 Oct;68(2):103-25. Review.

PMID:
10527663
13.

Heredity and strabismus.

Grützner IP, Yazawa K, Spivey BE.

Surv Ophthalmol. 1970 May;14(6):441-56. Review. No abstract available.

PMID:
4988135
14.

Clinical genetics: an overview.

Nehring WM, Faux SA.

J Cardiovasc Nurs. 1999 Jul;13(4):19-33. Review.

PMID:
10386269
15.

[Mucoviscidosis. New molecular biology knowledge and its significance for therapy].

Ecker-Schlipf B.

Med Monatsschr Pharm. 1993 Apr;16(4):114-6. Review. German. No abstract available.

PMID:
7683368
16.

Cystinosis.

Schulman JD.

Prog Clin Biol Res. 1989;305:137-44. Review. No abstract available.

PMID:
2668970
17.

[Hereditary optic atrophy].

Lorenz B.

Ophthalmologe. 1994 Dec;91(6):831-50. Review. German. No abstract available.

PMID:
7849440
18.

[New aspects on the pathogenesis of genetic hemochromatosis].

Stremmel W, Niederau C.

Z Gastroenterol. 1993 Nov;31 Suppl 5:46-8. Review. German. No abstract available.

PMID:
8197801
19.

Haemochromatosis: pathological or beneficial.

Worwood M.

Schweiz Med Wochenschr. 1998 Dec 5;128(49):1925-35. Review.

PMID:
9887470
20.

Gene therapy for phenylketonuria.

Eisensmith RC, Woo SL.

Acta Paediatr Suppl. 1994 Dec;407:124-9. Review.

PMID:
7766948
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