The Ohdo blepharophimosis syndrome: a third case.

Por Biesecker, L G
Publicado em 1991

What you can learn from one gene: GLI3

Por Biesecker, L G
Publicado em 2006

Pfeiffer type cardiocranial syndrome: a third case report.

Por Williamson-Kruse, L, Biesecker, L G
Publicado em 1995

Pallister-Hall syndrome.

Por Biesecker, L G, Graham, J M
Publicado em 1996

Internet solicitation of research subjects for genetic studies.

Por Biesecker, L G, DeRenzo, E G
Publicado em 1995

Identification of four murine cDNAs encoding putative protein kinases from primitive embryonic stem cells differentiated in vitro.

Por Biesecker, L G, Gottschalk, L R, Emerson, S G
Publicado em 1993

Mild phenotypic manifestation of a 7p15.3p21.2 deletion.

Por Wang, C, Maynard, S, Glover, T W, Biesecker, L G
Publicado em 1993

Familial Pallister-Hall syndrome.

Por Biesecker, L G, Topf, K, Graham, J M
Publicado em 1994

Pluripotent hematopoietic stem cells contain high levels of mRNA for c-kit, GATA-2, p45 NF-E2, and c-myb and low levels or no mRNA for c-fms and the receptors for granulocyte colon...

Por Orlic, D, Anderson, S, Biesecker, L G, Sorrentino, B P, Bodine, D M
Publicado em 1995

Defining personal utility in genomics: A Delphi study

Por Kohler, J.N., Turbitt, E., Lewis, K.L., Wilfond, B.S., Jamal, L., Peay, H.L., Biesecker, L.G., Biesecker, B.B.
Publicado no Clin Genet (2017)

Linkage mapping and phenotypic analysis of autosomal dominant Pallister-Hall syndrome.

Por Kang, S, Allen, J, Graham, J M, Grebe, T, Clericuzio, C, Patronas, N, Ondrey, F, Green, E, Schäffer, A, Abbott, M, Biesecker, L G
Publicado em 1997

Exclusion of candidate loci and cholesterol biosynthetic abnormalities in familial Pallister-Hall syndrome.

Por Biesecker, L G, Kang, S, Schäffer, A A, Abbott, M, Kelley, R I, Allen, J C, Clericuzio, C, Grebe, T, Olney, A, Graham, J M
Publicado em 1996

Molecular analysis of the 18q- syndrome--and correlation with phenotype.

Por Kline, A D, White, M E, Wapner, R, Rojas, K, Biesecker, L G, Kamholz, J, Zackai, E H, Muenke, M, Scott, C I, Overhauser, J
Publicado em 1993

Guidelines for investigating causality of sequence variants in human disease

Por MacArthur, D. G., Manolio, T. A., Dimmock, D. P., Rehm, H. L., Shendure, J., Abecasis, G. R., Adams, D. R., Altman, R. B., Antonarakis, S. E., Ashley, E. A., Barrett, J. C., Biesecker, L. G., Conrad, D. F., Cooper, G. M., Cox, N. J., Daly, M. J., Gerstein, M. B., Goldstein, D. B., Hirschhorn, J. N., Leal, S. M., Pennacchio, L. A., Stamatoyannopoulos, J. A., Sunyaev, S. R., Valle, D., Voight, B. F., Winckler, W., Gunter, C.
Publicado em 2014