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Federación Mexicana de Ginecología y Obstetricia, A.C.

2009, Number 01

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Ginecol Obstet Mex 2009; 77 (01)

Clinical practice guidelines 2008. Mexican College of Obstetrics and Gynecology Specialists

Language: Spanish
References: 28
Page: 1-25
PDF size: 242.74 Kb.


ABSTRACT

No abstract


REFERENCES

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  2. Báez R. Aspectos bioéticos del diagnóstico prenatal. Revista de Sanidad Militar 2008;62:42-9.

  3. Eugene C, Rich E, Burke W, Heaton C, et al. Reconsidering the family History in Primary Care. JGIM 2004;19:273-80.

  4. Van der Berg M, Timmermans D, Kleivend D, Van Eijk J, et al. Are counselor’s attitudes infl uencing pregnant woman’s attitudes and decisitions on prenatal screening? Prenat Diagn 2007;27:518-24.

  5. Bennet RL, Motulsky AG, Bittles A, Hudgins L, Uhrich S, et al. Genetic counseling and screening of consanguineous couples and their offspring: recommendations of the National Society of Genetic Counselors. J Genet Counsel 2007;11:97-119.

  6. Lisker R. Changing opinions of Mexican geneticists on ethical issues. Arch Med Res 2006;37:794-803.

  7. Bernhardt B, Biesecker B, Mastromarino C. Goals, Benefi ts, and Outcomes of Genetic Counseling: Client and Genetic Counselor Assessment. Am J of Med Gen 2000;94:189-97.

  8. Pinto-Escalante D, Ceballos-Quintal J, Castillo-Zapata I. Fundamentos actuales del asesoramiento genético. Rev Biomed 2001;12:186-95.

  9. Chodirker BN, Cadrin C, Davies GAL, Summers AM, Wilson RD, et al. Genetic Indications for Prenatal Diagnosis. J. Soc Obstet Gynaecol Can 2001;23:525-31.

  10. Mayén DG, Hernández C, Grether P. Actitud y aceptación de las mujeres embarazadas hacia el diagnóstico citogenético prenatal. Ginecología y Obstetricia de México 1997;65:107-10.

  11. Chen XK, Wen SW, Fleming N, Yang O, Walker MC. Teeage pregnancy and congenital anomalies: which system is vulne- rabl? Human Reprod 2007;22:1730-5.

  12. Yan Q, Wen SW, Leader A, Chen XK, et al. Paternal age and birth defects: how strong is the association ? Hum Reprod 2007;22:656-70.

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  14. Driscoll DA, Gross SJ. Professional Practice and Guidelines Committee. First trimester diagnosis and screening for fetal aneuploidy. Genet Med 2008;10:73-5.

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  16. David AL, Gouda V, Tembul C, Chtly ZC. The risk of recurence of holoprosencephaly in euploid fetuses. Obstet Gynecol 2007;110: 658-62.

  17. Joo JG, Beke A, Poop Z, Rob A, Poop C. Risk of recurrence in major central nervous system malfomations between 1976 and 2005. Birth 2007;27:1028-32.

  18. Tihy F, Lemieux N, Lenyre E. Complex chromosome rearrangement and recombinant balanced translocation in mother and daughter with the same phenotypic abnormalities. Am J Med Genet 2005;135:317-9.

  19. Shaw GM, Nelson V, Olshan. Paternal occupational group and risk of offspring with neural tube defects. Pediatr Perinatal Epidemiol 2002;16:328-33.

  20. Cicero S, Curcio P, Papageorghiou A, Sanek J, Nicolaides KH. Integrated ultrasound and biochemical screening for trisomy 21 at 11 to 14 weeks. Prenat Diagn 2003;23:306-10.

  21. Laurino MY, Bennett RL, Saraiya DS, Baumeister L, et al. Genetic evaluation and counseling of couples with recurrent miscarriage: recommendations of the National Society of Genetic Counselors. J Genet Counsel 2007;14:165-81.

  22. Finish Medical Society Duodecim. Systemic diseases in pregnancy. In: EBM Guidelines. Evidence-Based Medicine. Helsinki: John Wiley & Sons, 2006.

  23. European guidelines on cardiovascular disease prevention in clinical practice. Eur J Cardiovasc Prev Rehabil 2003;10:1-78.

  24. Royal College of Obstetricians and Gynaecologists. Alcohol consumption and the outcomes of pregnancy. RCOG Statement No. 5, 2006;pp:1-10.

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  28. Bener A, Hussain R, Teabi AS. Consanguineous marriages and their effects on common adult diseases: studies from an endogamous population. Med Princ Pract 2007;16:262-7.




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