1. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure;Aittomäki;Cell,1995
2. A gene for blepharophimosis-ptosis-epicanthus inversus syndrome maps to chromosome 3q22-q23;Amati;Hum. Genet.,1995
3. Barlow, C., Hirotsune, S., Paylor, R., Liyanage, M., Eckhaus, M., Collins, F., Shiloh Y., Crawley, J.N., Ried, T., Tagle, D., Wynshaw-Boris, A., 1996. Atm-deficient mice: a paradigm of Ataxia Telegiectasia. Cell 86, 159–71.
4. A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility;Bione;Am. J. Hum. Genet.,1998
5. Conway, G.S., Payne, N.N., Conway, E., Avey, C.J., Murray, A., Weeb, J., Jacobs, P.A., Simoni, M., Gromoll, J., Höppner, W., Nieschlag, E., 1997. A genetic study of familial and sporadic premature ovarian failure: screening for FSH mutations of the FSH receptor and ZFX genes and for FRAXA premutations. The Endocrine Society, 79th annual meeting abstract.