Morán-Barroso VF

Language: Spanish
References: 14
Page: 69-71
PDF size: 86.59 Kb.

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REFERENCES

1. Van Esch H, Fryns JF. Dysmorphism: syndromes. Encyclopedia of Life Sciences. New York: John Wiley & Sons, Ltd. www.els.net; 2005.

2. Canun–Serrano S. Detección de malformaciones congénitas externas. Bol Med Hosp Infant Mex. 1984; 41: 21-4.

3. Polifka JE, Friedman JM. Medical genetics: 1. Clinical teratology in the age of genomics. CMAJ. 2002; 167: 265-73.

4. Brent RL. Enviromental causes of human congenital malformations: the pediatrician’s role in dealing with these complex clinical problems caused by a multiplicity of environmental and genetic factor. Pediatrics. 2004; 113 Supl 4: 957-68.

5. Murguía-Peniche MT, Peña-Alonso YR, García-Delgado C. Lactante menor con malformaciones múltiples: hija de madre fumadora. Bol Med Hosp Infant Mex. 2007; 64:112-24.

6. Jacobs PA. Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding. J Med Genet. 1992; 29: 103-8.

7. Reis-Filho JS, Schmitt FCL. Fluorescence in situ hybridization, comparative genomic hybridization, and other molecular biology techniques in the analysis of effusions. Diagn Cytopathol. 2005; 33: 294-9.

8. Ingvarsson RF, Bjarnason AO, Dagbjartsson A. The effects of smoking in pregnancy on factors influencing fetal growth. Acta Pediatr. 2007; 96: 383-6.

9. Jaddoe VWV, Verburg BO, de Ridder MAJ. Maternal smoking and fetal growth characteristics I different periods of pregnancy. The generation R study. Am J Epidemiol. 2007; 165: 1207-15.

10. Honein MA, Rasmussen SA, Reefhuis J. Maternal smoking and environmental tobacco smoke exposure and the risk of orofacial clefts. Epidemiology. 2007; 18: 226-33.

11. Shi M, Christensen K, Weinberg CR. Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants. Am J Med Genet. 2007; 80: 76-90.

12. González-Ramos M. Consejo genético en la práctica clínica. Bol Med Hosp Infant Mex. 1985; 42: 402-6.

13. Weil J. Genetic counselling in the era of genomic medicine. As we move towards personalized medicine, it becomes more important to help patients understand genetic tests and make complex decisions about their health. EMBO Rep. 2002; 3: 590-3.

14. Wynshaw-Boris A. Inborn errors of development: disruption of pathways critical for normal development. Pediatr Clin North Am. 2006; 53: 855-71.