2005, Number 1
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Gac Med Mex 2005; 141 (1)
Molecular diagnosis in patients and carriers of Hemophilia A and B.
Mantilla-Capacho J, Beltrán-Miranda CP, Jaloma-Cruz AR
Language: Spanish
References: 5
Page: 69-72
PDF size: 31.80 Kb.
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REFERENCES
Haig H, Kazazian Jr. Hemophilia A: Deficiency of Coagulation Factor VIII. En: The metabolic basis of inherited disease. Scriver CR, Beaudet AL, Sly Ws, Valle D. (Eds). Mc Graw Hill. Inc. 8th. Edition, New York, 2001. p. 4367-4392.
Pollak ES and High KA. Hemophilia B: Factor IX Deficiency. En: The metabolic basis of inherited disease. Scriver CR, Beaudet AL, Sly Ws, Valle D. (Eds). Mc Graw-Hill. Inc. 8th. Edition New York, 2001, p. 4393-4413.
Peake IR, Lillicrap DP, Boulyjenkov V, Briet E, Chan V, Ginter EK, Kraus EM, Ljung R, Mannucci PM, Nicoladies K and Tuddenham EGD. Hemophilia: strategies for carrier detection and prenatal diagnosis. Bulletin of the World Health Organization, 1993; 71: 429-458.
Martínez-Gallegos R, Benítez-Arana H, Navarrete C, Peñaloza-Espinoza R, Salamanca-Gómez F, Arenas-Aranda D. Polymorphism distribution of Int13, Int22, and St14 VNTRs in a Mexican population and their application in carrier diagnosis of hemophilia A. Am J Hematol. 2004; 77: 1-6.
Jaloma-Cruz AR, Scaringe WA, Roberts S, Li S, Barros-Núñez P, Figuera LE, Rivas F, Cantú JM and Sommer SS. Nine independent F9 mutations in the Mexican hemophilia B population: Non-random recurrences of point mutation events in the human germline. Hum Mut. 2000; 15: 116-117.
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