Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita by REUTENS, A. T, ACHERMANN, J. C, ITO, Masafumi, ITO, Mika, GU, W.-X, HABIBY, R. L, DONOHOUE, P. A, SONGYA PANG, HINDMARSH, P. C, JAMESON, J. L

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Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delay by ACHERMANN, J. C, GU, W.-X, CROWLEY, W. F, LAYMAN, L. C, JAMESON, J. L, KOTLAR, T. J, MEEKS, J. J, SABACAN, L. P, SEMINARA, S. B, HABIBY, R. L, HINDMARSH, P. C, BICK, D. P, SHERINS, R. J

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A novel mutation (Q40p) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia : Evidence for phenotypic variability in mother and child by CONGDON, Tamara, NGUYEN, Lynda Q, NOGUEIRA, Celia R, HABIBY, Reema L, MEDEIROS-NETO, Geraldo, KOPP, Peter

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Adrenal hypoplasia congenita with hypogonadotropic hypogonadism. Evidence that DAX-1 mutations lead to combined hypothalamic and pituitary defects in gonadotropin production by Habiby, R L, Boepple, P, Nachtigall, L, Sluss, P M, Crowley, WF Jr, Jameson, J L

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A single-sample, subcutaneous gonadotropin-releasing hormone test for central precocious puberty by ECKERT, K. L, WILSON, D. M, BACHRACH, L. K, ANHALT, H, HABIBY, R. L, OLNEY, R. C, HINTZ, R. L, NEELY, E. K

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Missense mutations cluster within the carboxyl-terminal region of DAX-1 and impair transcriptional repression by ACHERMANNT, John C, ITO, Masafumi, SILVERMAN, Bernard L, HABIBY, Reema L, SONGYA PANG, ROSLER, Ariel, JAMESON, J. Larry

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Bone mineral density during treatment of central precocious puberty by Neely, E.Kirk, Bachrach, Laura K., Hintz, Raymond L., Habiby, Reema L., Slemenda, Charles W., Feezle, Lori, Pescovitz, Ora H.

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Presymptomatic diagnosis of X-linked adrenal hypoplasia congenita by analysis of DAX1 by Achermann, John C., Silverman, Bernard L., Habiby, Reema L., Jameson, J.Larry

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Adrenal hypoplasia congenita with hypogonadotropic hypogonadism: evidence that DAX-1 mutations lead to combined hypothalmic and pituitary defects in gonadotropin production by Habiby, R L, Boepple, P, Nachtigall, L, Sluss, P M, Crowley, Jr, W F, Jameson, J L

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A Novel Mutation (Q40P) in PAX8 Associated with Congenital Hypothyroidism and Thyroid Hypoplasia: Evidence for Phenotypic Variability in Mother and Child by Congdon, Tamara, Nguyen, Lynda Q., Nogueira, Celia R., Habiby, Reema L., Medeiros-Neto, Geraldo, Kopp, Peter

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Identification of 17 hearing impaired mouse strains in the TMGC ENU-mutagenesis screen by Habiby Kermany, Mohammad, Parker, Lisan L., Guo, Yun-Kai, Miller, Darla, Swanson, Douglas J., Yoo, Tai-June, Goldowitz, Dan, Zuo, Jian

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Wavelength-domain simulation of multiwavelength optical networks by Roudas, I., Antoniades, N., Richards, D.H., Wagner, R.E., Jackel, J.L., Habiby, S.F., Stern, T.E., Elrefaie, A.E.

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