Increased frequency of occult fragile X-associated primary ovarian insufficiency in infertile women with evidence of impaired ovarian function von Karimov, C.B., Moragianni, V.A., Cronister, A., Srouji, S., Petrozza, J., Racowsky, C., Ginsburg, E., Thornton, K.L., Welt, C.K.

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Abstract P2-09-21: HBOC genetic counseling: A genetic counselor-physician partnership model von Oliver, JB, Cronister, A

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Fragile X syndrome carrier screening in the prenatal genetic counseling setting von Cronister, Amy, DiMaio, Miriam, Mahoney, Maurice J., Donnenfeld, Alan E., Hallam, Stephanie

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O-46 von Cronister, A., Abrams, L., Mcconkie-Rosell, A., Gane, L., Finucane, B., Hagerman, R.J.

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O-46: Fragile X cascade testing and genetic counseling guidelines for patients seen in the infertility setting: A center for disease control and prevention, M.I.N.D Institute and N... von Cronister, A., Abrams, L., Mcconkie-Rosell, A., Gane, L., Finucane, B., Hagerman, R.J.

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Parental inheritance and psychological disability in fragile X females von REISS, A. L, FREUND, L, VINOGRADOV, S, HAGERMAN, R, CRONISTER, A

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Mental impairment in cytogenetically positive fragile X females von Cronister, Amy, Hagerman, Randi J., Wittenberger, Michael, Amiri, Khaled

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Fragile X checklist von Hagerman, Randi J., Amiri, Khaled, Cronister, Amy

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Heterozygous fragile X female: Historical, physical, cognitive, and cytogenetic features von Cronister, Amy, Schreiner, Rebecca, Wittenberger, Michael, Amiri, Khaled, Harris, Keri, Hagerman, Randi J.

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Direct mutation analysis of 495 patients for fragile X carrier status/proband diagnosis von Kaplan, Gail, Kung, Melissa, McClure, Melody, Cronister, Amy

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Oral-facial-digital syndrome type VI (Váradi syndrome): Further clinical delineation von Münke, Maximilian, McDonald, Donna M., Cronister, Amy, Stewart, Janet M., Gorlin, Robert J., Zackai, Elaine H.

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Dissemination of genetic risk information to relatives in the fragile X syndrome: Guidelines for genetic counselors von McConkie-Rosell, A., Robinson, H., Wake, S., Staley, L. W., Heller, K., Cronister, A.

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GIRLS WITH FRAGILE-X SYNDROME - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME von HAGERMAN, RJ, JACKSON, C, AMIRI, K, SILVERMAN, AC, OCONNOR, R, SOBESKY, W

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Specific Frontal Lobe Deficits among Women with the Fragile X Gene von MAZZOCCO, MICHÈLE M.M., HAGERMAN, RANDI J., CRONISTER-SILVERMAN, AMY, PENNINGTON, BRUCE F.

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Fragile X syndrome von Cronister, Amy Elizabeth, Hagerman, Randi Jenssen

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Direct mutation analysis of 495 patients for fragile X carriers status/proband diagnosis: X-linked mental retardation von KAPLAN, G, KUNG, M, MCCLURE, M, CRONISTER, A

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Expanding the role of the genetic counselor: X-Linked mental retardation. Part II von STALEY-GANE, L, FLYNN, L, NEITZEL, K, CRONISTER, A, HAGERMAN, R. J

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Expanding the role of the genetic counselor von Staley-Gane, Louise, Flynn, Linda, Neitzel, Kari, Cronister, Amy, Hagerman, Randi J.

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OP312 - A tale of two years: effects of a shift in genetic counseling modality on genetic testing uptake and follow-through von Bailey, Adrienne, Cronister, Amy, Oliver, Joan

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A tale of two years: effects of a shift in genetic counseling modality on genetic testing uptake and follow-through von Bailey, Adrienne, Cronister, Amy, Oliver, Joan

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