Variable expressivity of patched mutations in flies and humans.

Por Bale, A E
Publicado em 1997

Two RFLPs at the glutathione S-transferase 3 gene

Por Wong, E.L., Kandpal, G., Bale, A.E.
Publicado em 1990

Ornithine transcarbamylase polymorphism detected by PCR introduction of Dral site

Por Petty, E.M., Carstens, R., Bale, A.E.
Publicado em 1991

A retinoic acid receptor cDNA probe (RAR2) identifies a moderately frequent RFLP on chromosome 17.

Por Bale, A E, Weinberger, C, McBride, O W
Publicado em 1988

Six RFLPs for human T cell receptor alpha (TCRA) on chromosome 14.

Por Mitchell, A L, Bale, A E, Mak, T, McBride, O W
Publicado em 1989

Localization of the gene for the nevoid basal cell carcinoma syndrome.

Por Goldstein, A. M., Stewart, C., Bale, A. E., Bale, S. J., Dean, M.
Publicado em 1994

A cDNA probe (PheA12) from the hc-(ERBA) gene on chromosome 3 detects a high frequency RFLP.

Por Bale, A E, Usala, S, Weinberger, C, Weintraub, B D, McBride, O W
Publicado em 1988

Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland.

Por Petty, E. M., Green, J. S., Marx, S. J., Taggart, R. T., Farid, N., Bale, A. E.
Publicado em 1994

PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma.

Por Rosenberg, C L, Wong, E, Petty, E M, Bale, A E, Tsujimoto, Y, Harris, N L, Arnold, A
Publicado em 1991

Alcohol intake and early-onset basal cell carcinoma in a case-control study

Por Zhang, Y, Ferrucci, L.M., Cartmel, B., Molinaro, A.M., Leffell, D.J., Bale, A.E., Mayne, S.T.
Publicado no Br J Dermatol (2014)

Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s).

Por Petty, E M, Gibson, L H, Fountain, J W, Bolognia, J L, Yang-Feng, T L, Housman, D E, Bale, A E
Publicado em 1993

Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients.

Por Shimkets, R., Gailani, M. R., Siu, V. M., Yang-Feng, T., Pressman, C. L., Levanat, S., Goldstein, A., Dean, M., Bale, A. E.
Publicado em 1996

Nephrogenic diabetes insipidus: an X chromosome-linked dominant inheritance pattern with a vasopressin type 2 receptor gene that is structurally normal.

Por Friedman, E, Bale, A E, Carson, E, Boson, W L, Nordenskjöld, M, Ritzén, M, Ferreira, P C, Jammal, A, De Marco, L
Publicado em 1994

Human CYP1A1 gene: cosegregation of the enzyme inducibility phenotype and an RFLP.

Por Petersen, D D, McKinney, C E, Ikeya, K, Smith, H H, Bale, A E, McBride, O W, Nebert, D W
Publicado em 1991

A base mutation of the C-erbA beta thyroid hormone receptor in a kindred with generalized thyroid hormone resistance. Molecular heterogeneity in two other kindreds.

Por Usala, S J, Tennyson, G E, Bale, A E, Lash, R W, Gesundheit, N, Wondisford, F E, Accili, D, Hauser, P, Weintraub, B D
Publicado em 1990

Mutation hotspots due to sunlight in the p53 gene of nonmelanoma skin cancers.

Por Ziegler, A, Leffell, D J, Kunala, S, Sharma, H W, Gailani, M, Simon, J A, Halperin, A J, Baden, H P, Shapiro, P E, Bale, A E
Publicado em 1993

Progesterone receptor variation and risk of ovarian cancer is limited to the invasive endometrioid subtype: results from the ovarian cancer association consortium pooled analysis

Por Pearce, C L, Wu, A H, Gayther, S A, Bale, A E, Beck, P A, Beesley, J, Chanock, S, Cramer, D W, DiCioccio, R, Edwards, R, Fredericksen, Z S, Garcia-Closas, M, Goode, E L, Green, A C, Hartmann, L C, Hogdall, E, Kjær, S K, Lissowska, J, McGuire, V, Modugno, F, Moysich, K, Ness, R B, Ramus, S J, Risch, H A, Sellers, T A, Song, H, Stram, D O, Terry, K L, Webb, P M, Whiteman, D C, Whittemore, A S, Zheng, W, Pharoah, P D P, Chenevix-Trench, G, Pike, M C, Schildkraut, J, Berchuck, A
Publicado em 2008