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2.Bridge PJ. The calculation of Genetic Risks. The John Hopkins University Press. Baltimore. 1994.

3.British Medical Journal Publising Group. Basic Molecular and Cell Biology. Segunda Edición.. London. 1993.

4.Brock DJH. Molecular Genetics for the Clinician. Cambridge University Press. Cambridge. 1993

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10.Primrose SB. Principles of Genome Analysis. Blackwell Science Ltd. Oxford. 1995

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Citas Bibliograficas de otros articulos:

Biología Molecular y Medicina: Conceptos Básicos.
Silvana Zanlungo, Attilio Rigotti, Marco Arrese.
Publicado en: Revista Médica de Chile, 1999;127:839-847

1.Anand, R. Techniques for the Analysis of Complex Genomes. Academic Press, London. (1992).

2.Green, E. D., Cox, D. R. & Myers, R. M. (1995). The human genome project and its impact on the study of human disease. In: The metabolic and molecular basis of inherited disease C.R. Scriver, A. L. Beaudet, W. S. Sly & D.Valle (eds.), McGraw-Hill, New York. pp. 401-436.

3.Kreuzer H, Massey A. Recombinant ADN and biotechnology. A guide for teachers. ASM Press, Washington D.C. (1996).

4.Hayes,JD, Stockman PK. Electrophoresis of proteins and nucleicacids: I-Theory. Br Med Journal 1989;299:843-846.

5.Hayes,JD, Stockman PK. Electrophoresis of proteins and nucleic acids: II-Techniques and applications. Br Med Journal 1989;299:907-910.

6.Hayes PC, Wolf RC, Hayes JD. (1989). Blotting techniques for the study of ADN, RNA and proteins. Br Med Journal 1989;299:965-968.

7.Ballabio A, Jameson JL. Introduction to molecular medicine. In: Jameson JL (ed.). Principles of Molecular Medicine. Humana Press, Totowa, New Yersey, USA, 1998, pp. 3-97.

Identificación de Defectos Moleculares en las Enfermedades Hepáticas: Algunos ejemplos recientes..

Marco Arrese
Publicado en: Revista Médica de Chile, 1999;127
1.Iyanagi T, Emi Y, Ikushiro S. Biochemical and molecular aspects of genetic disorders of bilirubin metabolism. Biochim Biophys Acta 1998 Sep 30;1407(3):173-84

2.Bacon BR, Powell LW, Adams PC, Kresina TF, Hoofnagle JH. Molecular medicine and hemochromatosis: at the crossroads. Gastroenterology 1999;116:193-207

3.Cuthbert JA. Wilson's disease. Update of a systemic disorder with protean manifestations. Gastroenterol Clin North Am. 1998;27:655-81.

4.Miranda M, Brinck P, Roessler JL, Troncoso Sch M, Gonzalez M, Alarcon T, Villagra R. Wilson's disease: a review apropos of a clinical experience in 16 patients. Rev Med Chil 1995;123:1098-107

5.Arrese M, Ananthananarayanan M, Suchy FJ. Hepatobiliary transport: molecular mechanisms of development and cholestasis. Pediatr Res 1998;44:141-7

6.Shneider BL. Genetic cholestasis syndromes. J Pediatr Gastroenterol Nutr 1999;28:124-31

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