3 results for author:"Habiby R.L." in Literature citations
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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. Congdon T., Nguyen L.Q., Nogueira C.R., Habiby R.L., Medeiros-Neto G., Kopp P. J. Clin. Endocrinol. Metab. 86:3962-3967(2001) · UniProtKB (1) |
| Missense mutations cluster within the carboxyl-terminal region of DAX-1 and impair transcriptional repression. Achermann J.C., Ito M., Silverman B.L., Habiby R.L., Pang S., Rosler A., Jameson J.L. J. Clin. Endocrinol. Metab. 86:3171-3175(2001) · UniProtKB (1) |
| Presymptomatic diagnosis of X-linked adrenal hypoplasia congenita by analysis of DAX1. Achermann J.C., Silverman B.L., Habiby R.L., Jameson J.L. J. Pediatr. 137:878-881(2000) · UniProtKB (1) |