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PUBMED FOR HANDHELDS

Journal Abstract Search


126 related items for PubMed ID: 4356121

  • 21.
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  • 24. Familial hyperphosphatasemia with ateliosis and hypermetabolism of growing membranous bone; review of the clinical, radiographic and chemical features.
    Caffey J.
    Bull Hosp Joint Dis; 1972 Oct; 33(2):81-110. PubMed ID: 4648260
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  • 25.
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  • 26. Mannosidosis in three brothers--a review of the literature.
    Vidgoff J, Lovrien EW, Beals RK, Buist NR.
    Medicine (Baltimore); 1977 Jul; 56(4):335-48. PubMed ID: 875720
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  • 27. Detection of heterozygotes for aspartylglucosaminuria (AGU) in cultured fibroblasts.
    Aula P, Autio S, Raivio K, Näntö V.
    Humangenetik; 1974 Jul; 25(4):307-14. PubMed ID: 4464238
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  • 28. A search for aspartylglycosaminuria in Poland.
    Galewicz A, Gorska D, Rodo M, Zaremba J.
    J Ment Defic Res; 1974 Jun; 18(2):135-7. PubMed ID: 4449118
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  • 30. Clinical and aetiological study of childhood mental retardation.
    Subrahmanyam G, Agarwal KN, Agrawal SP, Jaiswal A.
    Indian Pediatr; 1974 Nov; 11(11):723-7. PubMed ID: 4475031
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  • 32. Alpha-1-antitrypsin deficiency and disease.
    Alper CA, Johnson AM.
    Pediatrics; 1970 Dec; 46(6):837-40. PubMed ID: 4923511
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  • 33. Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristics.
    Gehler J, Sewell AC, Becker C, Spranger J, Hartmann J.
    J Inherit Metab Dis; 1981 Dec; 4(4):229-30. PubMed ID: 6796777
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  • 35. Pattern of inborn errors of metabolism in an Omani population of the Arabian Peninsula.
    Joshi SN, Hashim J, Venugopalan P.
    Ann Trop Paediatr; 2002 Mar; 22(1):93-6. PubMed ID: 11926058
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  • 36. [Peroxisomal disorders--DNA analysis].
    Orii T, Suzuki Y, Shimozawa N, Yajima S, Asano J.
    Nihon Rinsho; 1993 Jan; 51 Suppl():1068-77. PubMed ID: 8096253
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  • 40. Glyceroluria in healthy adults, mentally ill adults and children selected for metabolic screening.
    Kohlschütter A, Seitz HJ, Feldmann B, Lehnert W, Langenbeck U.
    Clin Chim Acta; 1991 May 15; 198(3):203-7. PubMed ID: 1889122
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