Frequencies of cystic fibrosis mutations in the Maine population : high proportion of unknown alleles in individuals of French-Canadian ancestry von BAYLERAN, J. K, YAN, H, HOPPER, C. A, SIMPSON, E. M

Volltext

Severe factor VII deficiency due to a mutation disrupting a hepatocyte nuclear factor 4 binding site in the factor VII promoter von ARBINI, A. A, POLLAK, E. S, BAYLERAN, J. K, HIGH, K. A, BAUER, K. A

Volltext

A Combined Cytogenetic and Molecular Approach for Diagnosing Delayed Puberty von Hon Fong Louie Mark, Bayleran, Janet K., Seifer, David B., Meyers-Seifer, Cynthia H.

Volltext

Intron/exon structure confirms that mouse Zfy1 and Zfy2 are members of the ZFY gene family von MAHAFFEY, C. L, BAYLERAN, J. K, YEH, G. Y, LEE, T. C, PAGE, D. C, SIMPSON, E. M

Volltext

An expanded collection of mouse Y chromosome RDA clones von Bergstrom, D E, Yan, H, Sonti, M M, Narayanswami, S, Bayleran, J K, Simpson, E M

Volltext

Severe Factor VII Deficiency Due to a Mutation Disrupting a Hepatocyte Nuclear Factor 4 Binding Site in the Factor VII Promoter von Arbini, Arnaldo A., Pollak, Eleanor S., Bayleran, Janet K., High, Katherine A., Bauer, Kenneth A.

Volltext

Novel Sxr super(a) ES Cell Line Offers Hope for Y Chromosome Gene-Targeted Mice von Simpson, E M, Johnson, KA, Shirley, B-J, Fang, Ge Y, Bayleran, J K, Lerner, C P

Volltext

Novel Sxr(a) ES cell line offers hope for Y chromosome gene-targeted mice von Simpson, Elizabeth M, Johnson, Kevin A, Shirley, Bobbi-Jo, Fang, Ge Y, Bayleran, Janet K, Lerner, Charles P

Volltext

Tay-Sachs disease: B 1 variant von Gordon, Bruce A., Gordon, Kevin E., Hinton, George G., Cadera, Werner, Feleki, Vera, Bayleran, Janet, Hechtman, Peter

Volltext

Tay-Sachs disease: B1 variant von Gordon, B A, Gordon, K E, Hinton, G G, Cadera, W, Feleki, V, Bayleran, J, Hechtman, P

Volltext