Variable expressivity of patched mutations in flies and humans.

Tekijä Bale, A E
Julkaistu 1997

Two RFLPs at the glutathione S-transferase 3 gene

Tekijä Wong, E.L., Kandpal, G., Bale, A.E.
Julkaistu 1990

Ornithine transcarbamylase polymorphism detected by PCR introduction of Dral site

Tekijä Petty, E.M., Carstens, R., Bale, A.E.
Julkaistu 1991

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

Tekijä Bale, A E, Weinberger, C, McBride, O W
Julkaistu 1988

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

Tekijä Mitchell, A L, Bale, A E, Mak, T, McBride, O W
Julkaistu 1989

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

Tekijä Goldstein, A. M., Stewart, C., Bale, A. E., Bale, S. J., Dean, M.
Julkaistu 1994

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

Tekijä Bale, A E, Usala, S, Weinberger, C, Weintraub, B D, McBride, O W
Julkaistu 1988

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

Tekijä Petty, E. M., Green, J. S., Marx, S. J., Taggart, R. T., Farid, N., Bale, A. E.
Julkaistu 1994

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

Tekijä Rosenberg, C L, Wong, E, Petty, E M, Bale, A E, Tsujimoto, Y, Harris, N L, Arnold, A
Julkaistu 1991

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

Tekijä Zhang, Y, Ferrucci, L.M., Cartmel, B., Molinaro, A.M., Leffell, D.J., Bale, A.E., Mayne, S.T.
Julkaisussa 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).

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

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

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

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

Tekijä Friedman, E, Bale, A E, Carson, E, Boson, W L, Nordenskjöld, M, Ritzén, M, Ferreira, P C, Jammal, A, De Marco, L
Julkaistu 1994

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

Tekijä Petersen, D D, McKinney, C E, Ikeya, K, Smith, H H, Bale, A E, McBride, O W, Nebert, D W
Julkaistu 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.

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

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

Tekijä 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
Julkaistu 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

Tekijä 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
Julkaistu 2008