Practice Guidelines

Cancer Risk

Trepanier, A., Ahrens, M., McKinnon, W., Peters, J., Stopfer, J., Grumet, S.C., et al. (2004). Genetic cancer risk assessment and counseling: Recommendations of the National Society of Genetic Counselors. J Genet Couns,13(2): 83-114.
http://www.springerlink.com/link.asp?id=v053u7467071k047

Consanguinity

Bennett, R.L., Motulsky, A.G., Bittles, A., Hudgins, L., Uhrich, S., Doyle, D.L., et al. (2002). Genetic counseling and screening of consanguineous couples and their offspring: Recommendations of the National Society of Genetic Counselors. J Genet Couns,11(2): 97-119.
http://www.springerlink.com/link.asp?id=uxwm5qr18j5lgrdt

Cystic Fibrosis

Langfelder-Schwind, E., Kloza, E., Sugarman, E., Pettersen, B., NSGC Subcommittee on Cystic Fibrosis Carrier Testing, Brown, T., et al. (2005). Cystic fibrosis prenatal screening in genetic counseling practice: Recommendations of the National Society of Genetic Counselors. J Genet Couns,14(1): 1-15.
http://www.springerlink.com/link.asp?id=g3813123744716h4

Fabry Disease

Bennett, R.L., Hart, K.A., O’Rourke, E., Barranger, J.A., Johnson, J., MacDermot, K.D., et al. (2002). Fabry disease in genetic counseling practice: Recommendations of the National Society of Genetic Counselors. J Genet Couns,11(2): 121-146.
http://www.springerlink.com/link.asp?id=pd2ejhrnrwtxac20

Fragile X Syndrome (coming soon)

McConkie-Rosell, A., Finucane, B., Cronister, A., Abrams, L., Bennett, R.L., & Pettersen, B.J. (2005). Genetic counseling for Fragile X syndrome: Updated recommendations of the National Society of Genetic Counselors. J Genet Couns,14(4): 249-270.
http://www.springerlink.com/link.asp?id=r54356r13r0740u7

Hereditary Breast and Ovarian Cancer

Berliner, J., Fay, A.M. (2007). Risk Assessment and Genetic Counseling for Hereditary Breast and Ovarian Cancer: Recommendations of the National Society of Genetic Counselors. J. Genet Couns, Online First
http://www.springerlink.com/link.asp?id=t01m017w16412k57

Human Pedigree Nomenclature

Bennett, R.L., Steinhaus, K.A., Uhrich, S.B., O’Sullivan, C.K., Resta, R.G., Lochner-Doyle, D., et al. (1995). Recommendations for standardized human pedigree nomenclature. J Genet Couns, 4(4): 267-279.
http://www.springerlink.com/link.asp?id=p5rh572228jl3557

Neurofibromatosis Type 1

Radtke, H.B., Sebold, C.D., Allison, C., Larsen Haidle, J., Schneider, G. (2007). Neurofibromatosis Type 1 in Genetic Counseling Practice: Recommendations of the National Society of Genetic Counselors. J Genet Couns, 16(3):
http://www.springerlink.com/link.asp?id=0365g21w57351w87

Recurrent Miscarriage

Laurino, M.Y., Bennett, R.L., Saraiya, D.S., Baumeister, L., Doyle D.L., Leppig, K., et al. (2005). Genetic counseling and evaluation of couples with recurrent miscarriage: Recommendations of the National Society of Genetic Counselors. J Genet Couns,14(3): 165-181.
http://www.springerlink.com/link.asp?id=m860387p16042986