28 related articles for article (PubMed ID: 113163)
21. Post- and pre-natal assessment of alpha-L-iduronidase deficiency with a radiolabelled natural substrate.
Hopwood JJ; Muller V; Pollard AC
Clin Sci (Lond); 1979 Jan; 56(6):591-9. PubMed ID: 113163
[No Abstract] [Full Text] [Related]
22. The clinical spectrum of alpha-L-iduronidase deficiency.
Roubicek M; Gehler J; Spranger J
Am J Med Genet; 1985 Mar; 20(3):471-81. PubMed ID: 3922223
[TBL] [Abstract][Full Text] [Related]
23. [Possible genetic nature of phenotypical differences of mucopolysaccharidosis 1].
Kobrinskiĭ BA
Vopr Med Khim; 1982; 28(3):55-7. PubMed ID: 6808766
[No Abstract] [Full Text] [Related]
24. A nonpathologic allele (IW) for low alpha-L-iduronidase enzyme activity vis-a-vis prenatal diagnosis of Hurler syndrome.
Whitley CB; Gorlin RJ; Krivit W
Am J Med Genet; 1987 Sep; 28(1):233-43. PubMed ID: 3118714
[TBL] [Abstract][Full Text] [Related]
25. Mucopolysaccharidoses and mucolipidoses.
Van Hoof F
J Clin Pathol Suppl (R Coll Pathol); 1974; 8():64-93. PubMed ID: 4220223
[No Abstract] [Full Text] [Related]
26. The biochemical basis for mucopolysaccharidoses and mucolipidoses.
Neufeld EF
Prog Med Genet; 1974; 10():81-101. PubMed ID: 4283415
[No Abstract] [Full Text] [Related]
27.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
28.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [New Search]
