Generation of glucocorticoid-responsive Moloney murine leukemia virus by insertion of regulatory sequences from murine mammary tumor virus into the long terminal repeat.

Por Overhauser, J, Fan, H
Publicado em 1985

No evidence for imprinting in distal 18q

Por MAIWALD, R., OVERHAUSER, J., LACCONE, F.
Publicado em 2000

A highly polymorphic locus in 5p15.2-5p15.3 (213-274EC) revealed by an anonymous single copy DNA fragment.

Por Overhauser, J, Beaudet, A L, Wasmuth, J J
Publicado em 1987

Identification of 28 DNA fragments that detect RFLPs in 13 distinct physical regions of the short arm of chromosome 5.

Por Overhauser, J, McMahan, J, Wasmuth, J J
Publicado em 1987

A fine structure physical map of the short arm of chromosome 5.

Por Overhauser, J, Beaudet, A L, Wasmuth, J J
Publicado em 1986

Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3.

Por Boghosian-Sell, L., Comings, D. E., Overhauser, J.
Publicado em 1996

Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype.

Por Overhauser, J, Golbus, M S, Schonberg, S A, Wasmuth, J J
Publicado em 1986

5p14 deletion associated with microcephaly and seizures

Por Johnson, E., Marinescu, R, Punnett, H., Tenenholz, B., Overhauser, J.
Publicado em 2000

A new deletion of 18q23 with few typical features of the 18q- syndrome.

Por Kohonen-Corish, M, Strathdee, G, Overhauser, J, McDonald, T, Jammu, V
Publicado em 1996

Interstitial deletions are not the main mechanism leading to 18q deletions.

Por Strathdee, G., Harrison, W., Riethman, H. C., Goodart, S. A., Overhauser, J.
Publicado em 1994

Transformation properties of type 5 adenovirus mutants that differentially express the E1A gene products.

Por Haley, K P, Overhauser, J, Babiss, L E, Ginsberg, H S, Jones, N C
Publicado em 1984

Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18.

Por Mewar, R, Kline, A D, Harrison, W, Rojas, K, Greenberg, F, Overhauser, J
Publicado em 1993

Evidence for a distinct region causing a cat-like cry in patients with 5p deletions.

Por Gersh, M, Goodart, S A, Pasztor, L M, Harris, D J, Weiss, L, Overhauser, J
Publicado em 1995

Targeted insertions of two exogenous collagen genes into both alleles of their endogenous loci in cultured human cells: the insertions are directed by relatively short fragments co...

Por Ganguly, A, Smelt, S, Mewar, R, Fertala, A, Sieron, A L, Overhauser, J, Prockop, D J
Publicado em 1994

Physical mapping of the holoprosencephaly critical region in 18p11.3.

Por Overhauser, J, Mitchell, H F, Zackai, E H, Tick, D B, Rojas, K, Muenke, M
Publicado em 1995

Molecular characterization of patients with 18q23 deletions.

Por Strathdee, G, Sutherland, R, Jonsson, J J, Sataloff, R, Kohonen-Corish, M, Grady, D, Overhauser, J
Publicado em 1997

Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5.

Por Overhauser, J, Bengtsson, U, McMahon, J, Ulm, J, Butler, M G, Santiago, L, Wasmuth, J J
Publicado em 1989

The first three mosaic cri du chat syndrome patients with two rearranged cell lines

Por PERFUMO, C, MAINARDI, P, CALI, A, COUCOURDE, G, ZARA, F, CAVANI, S, OVERHAUSER, J, BRICARELLI, F, PIERLUIGI, M
Publicado em 2000

Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation

Por Mainardi, P, Perfumo, C, Cali, A, Coucourde, G, Pastore, G, Cavani, S, Zara, F, Overhauser, J, Pierluigi, M, Bricarelli, F
Publicado em 2001

Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18.

Por Boghosian-Sell, L., Mewar, R., Harrison, W., Shapiro, R. M., Zackai, E. H., Carey, J., Davis-Keppen, L., Hudgins, L., Overhauser, J.
Publicado em 1994