“How Should I Tell my Child?” Disclosing the Diagnosis of Sex Chromosome Aneuploidies
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Link
http://link.springer.com/content/pdf/10.1007/s10897-014-9741-4
Reference25 articles.
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3. Borelli, J. B., Bender, B. G., Puck, M. H., Salbenblatt, J. A., & Robinson, A. (1984) . The meaning of early knowledge of a child’s infertility in families with 47, XXY and 45,X children. Child Psychiatry and Human Development, 14(4), 215–222.
4. Coffee, B., Keith, K., Albizua, I., Malone, T., Mowrey, J., Sherman, S. L., et al. (2009) . Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA. American Journal of Human Genetics, 85(4), 503–514.
5. Gallo, A., Angst, D., Knafl, K.A., Hadley, E. & Smith, C. (2005) . Parents sharing information with their children about genetic conditions. Journal of Pediatric Health Care, 267–275.
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