Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements.

Bằng Hecht, F, Kimberling, W J
Được phát hành 1971

Localization of spherocytosis to chromosome 8 or 12 and report of a family with spherocytosis and a reciprocal translocation.

Bằng Kimberling, W J, Fulbeck, T, Dixon, L, Lubs, H A
Được phát hành 1975

Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1.

Bằng Kumar, S, Kimberling, W J, Gabow, P A, Shugart, Y Y, Pieke-Dahl, S
Được phát hành 1990

Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications.

Bằng Kumar, S, Deffenbacher, K, Marres, H A, Cremers, C W, Kimberling, W J
Được phát hành 2000

Familial atypical multiple mole-melanoma (FAMMM) syndrome: segregation analysis.

Bằng Lynch, H T, Fusaro, R M, Kimberling, W J, Lynch, J F, Danes, B S
Được phát hành 1983

Genetic heterogeneity of Usher syndrome type II in a Dutch population.

Bằng Pieke-Dahl, S, van Aarem, A, Dobin, A, Cremers, C W, Kimberling, W J
Được phát hành 1996

Breast cancer, genetics, and age at first pregnancy.

Bằng Lynch, H T, Albano, W A, Layton, M A, Kimberling, W J, Lynch, J F
Được phát hành 1984

Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping.

Bằng Kumar, S., Kimberling, W. J., Connolly, C. J., Tinley, S., Marres, H. A., Cremers, C. W.
Được phát hành 1994

Phenotypic variation in the familial atypical multiple mole-melanoma syndrome (FAMMM).

Bằng Lynch, H T, Fusaro, R M, Albano, W A, Pester, J, Kimberling, W J, Lynch, J F
Được phát hành 1983

Mutation Profile of the CDH23 Gene in 56 Probands with Usher Syndrome Type I

Bằng Oshima, A., Jaijo, T., Aller, E., Millan, J.M., Carney, C., Usami, S., Moller, C., Kimberling, W.J.
Được phát hành 2008

Genetic heterogeneity of Usher syndrome type II.

Bằng Pieke Dahl, S, Kimberling, W J, Gorin, M B, Weston, M D, Furman, J M, Pikus, A, Möller, C
Được phát hành 1993

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.

Bằng Kelley, P M, Harris, D J, Comer, B C, Askew, J W, Fowler, T, Smith, S D, Kimberling, W J
Được phát hành 1998

Double aneuploidy: the frequency of XXY in males with Down's syndrome.

Bằng Hecht, F, Nievaard, J E, Duncanson, N, Miller, J R, Higgins, J V, Kimberling, W J, Walker, F A, Smith, G S, Thuline, H C, Tischler, B
Được phát hành 1969

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele

Bằng Varga, R, Avenarius, M R, Kelley, P M, Keats, B J, Berlin, C I, Hood, L J, Morlet, T G, Brashears, S M, Starr, A, Cohn, E S, Smith, R J H, Kimberling, W J
Được phát hành 2006

Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.

Bằng Weston, M. D., Kelley, P. M., Overbeck, L. D., Wagenaar, M., Orten, D. J., Hasson, T., Chen, Z. Y., Corey, D., Mooseker, M., Sumegi, J., Cremers, C., Moller, C., Jacobson, S. G., Gorin, M. B., Kimberling, W. J.
Được phát hành 1996

CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness

Bằng Astuto, L. M., Bork, J. M., Weston, M. D., Askew, J. W., Fields, R. R., Orten, D. J., Ohliger, S. J., Riazuddin, S., Morell, R. J., Khan, S., Riazuddin, S., Kremer, H., van Hauwe, P., Moller, C. G., Cremers, C. W. R. J., Ayuso, C., Heckenlively, J. R., Rohrschneider, K., Spandau, U., Greenberg, J., Ramesar, R., Reardon, W., Bitoun, P., Millan, J., Legge, R., Friedman, T. B., Kimberling, W. J.
Được phát hành 2002