Insulin-dependent diabetes mellitus: a model for the study of multifactorial disorders.

Por Field, L L
Publicado em 1988

Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.

Por Field, L L, Kaplan, B J
Publicado em 1998

SacI RFLP recognized by a human immunoglobulin kappa light chain constant region probe.

Por Field, L L, Tobias, R, Bech-Hansen, T
Publicado em 1987

Nonsyndromic cleft lip with or without cleft palate in west Bengal, India: evidence for an autosomal major locus.

Por Ray, A K, Field, L L, Marazita, M L
Publicado em 1993

Interaction between T cell receptor beta chain and immunoglobulin heavy chain region genes in susceptibility to insulin-dependent diabetes mellitus.

Por Field, L L, Stephure, D K, McArthur, R G
Publicado em 1991

Maternal uniparental disomy of chromosome 1 with no apparent phenotypic effects.

Por Field, L L, Tobias, R, Robinson, W P, Paisey, R, Bain, S
Publicado em 1998

Murine Pancreatic Beta TC3 Cells Show Greater 2′, 5′-Oligoadenylate Synthetase (2′5′AS) Antiviral Enzyme Activity and Apoptosis Following IFN-α or Poly(I:C) Treatment than Pancreat...

Por Li, M., Zheng, D. -J., Field, L. L., Bonnevie-Nielsen, V.
Publicado em 2009

HLA-dependent GM effects in insulin-dependent diabetes: evidence from pairs of affected siblings.

Por Field, L L, Dizier, M H, Anderson, C E, Spence, M A, Rotter, J I
Publicado em 1986

Linkage analysis of neurofibromatosis (von Recklinghausen disease).

Por Spence, M A, Bader, J L, Parry, D M, Field, L L, Funderburk, S J, Rubenstein, A E, Gilman, P A, Sparkes, R S
Publicado em 1983

Association mapping of disease loci, by use of a pooled DNA genomic screen.

Por Barcellos, L F, Klitz, W, Field, L L, Tobias, R, Bowcock, A M, Wilson, R, Nelson, M P, Nagatomi, J, Thomson, G
Publicado em 1997

Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosa.

Por Field, L L, Heckenlively, J R, Sparkes, R S, Garcia, C A, Farson, C, Zedalis, D, Sparkes, M C, Crist, M, Tideman, S, Spence, M A
Publicado em 1982

Association of the ROBO1 gene with reading disabilities in a family-based analysis

Por Tran, C., Wigg, K. G., Zhang, K., Cate-Carter, T. D., Kerr, E., Field, L. L., Kaplan, B. J., Lovett, M. W., Barr, C. L.
Publicado no Genes Brain Behav (2014)

The Tay-Sachs disease gene in North American Jewish populations: geographic variations and origin.

Por Petersen, G M, Rotter, J I, Cantor, R M, Field, L L, Greenwald, S, Lim, J S, Roy, C, Schoenfeld, V, Lowden, J A, Kaback, M M
Publicado em 1983

A Family-Based Association Analysis and Meta-Analysis of the Reading Disabilities Candidate Gene DYX1C1

Por Tran, C., Gagnon, F., Wigg, K.G., Feng, Y., Gomez, L., Cate-Carter, T.D., Kerr, E.N., Field, L.L., Kaplan, B.J., Lovett, M.W., Barr, C.L.
Publicado no Am J Med Genet B Neuropsychiatr Genet (2013)

Association of AXIN2 with Non-syndromic Oral Clefts in Multiple Populations

Por Letra, A., Bjork, B., Cooper, M.E., Szabo-Rogers, H., Deleyiannis, F.W.B., Field, L.L., Czeizel, A.E., Ma, L., Garlet, G.P., Poletta, F.A., Mereb, J.C., Lopez-Camelo, J.S., Castilla, E.E., Orioli, I.M., Wendell, S., Blanton, S.H., Liu, K., Hecht, J.T., Marazita, M.L., Vieira, A.R., Silva, R.M.
Publicado em 2012