Effect of defective interfering particles on plus- and minus- strand leader RNAs in vesicular stomatitis virus-infected cells.

Por Leppert, M, Kolakofsky, D
Publicado em 1980

5' Terminus of defective and nondefective Sendai viral genomes is ppp Ap.

Por Leppert, M, Kolakofsky, D
Publicado em 1978

Cytogenetic and molecular analysis of sex-chromosome monosomy.

Por Hassold, T, Benham, F, Leppert, M
Publicado em 1988

Determination of the parental origin of sex-chromosome monosomy using restriction fragment length polymorphisms.

Por Hassold, T, Kumlin, E, Takaesu, N, Leppert, M
Publicado em 1985

An anonymous single-copy clone, p30-1-60, identifies a frequent RFLP on chromosome 3p [HGM9 no. D3S86].

Por Litt, M, Litt, R, Ballard, L, Leppert, M
Publicado em 1989

Cytogenetic and molecular studies of trisomy 13.

Por Hassold, T, Jacobs, P A, Leppert, M, Sheldon, M
Publicado em 1987

Recessive inheritance of obesity in familial non-insulin-dependent diabetes mellitus, and lack of linkage to nine candidate genes.

Por Hasstedt, S J, Hoffman, M, Leppert, M F, Elbein, S C
Publicado em 1997

A CA repeat 30–70 KB downstream from the adenomatous polyposis coli (APC) gene

Por Spirio, L., Joslyn, G., Nelson, L., Leppert, M., White, R.
Publicado em 1991

Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity.

Por Heath, H, Jackson, C E, Otterud, B, Leppert, M F
Publicado em 1993

Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1.

Por German, J, Roe, A M, Leppert, M F, Ellis, N A
Publicado em 1994

Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.

Por Ptacek, L J, Tyler, F, Trimmer, J S, Agnew, W S, Leppert, M
Publicado em 1991

Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome.

Por Naumova, A K, Leppert, M, Barker, D F, Morgan, K, Sapienza, C
Publicado em 1998

A CA-repeat polymorphism close to the adenomatous polyposis coli (APC) gene offers improved diagnostic testing for familial APC.

Por Spirio, L, Nelson, L, Ward, K, Burt, R, White, R, Leppert, M
Publicado em 1993

Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11.

Por Keating, M, Dunn, C, Atkinson, D, Timothy, K, Vincent, G M, Leppert, M
Publicado em 1991

Characterization of a human 'midisatellite' sequence.

Por Nakamura, Y, Julier, C, Wolff, R, Holm, T, O'Connell, P, Leppert, M, White, R
Publicado em 1987

D7S448 detects a HindIII polymorphism located in the centromere region of chromosome 7

Por Dean, M., Stewart, C., Perry, A., Stauffer, D., Otterud, B., White, R., Leppert, M.
Publicado em 1991

Precise localization of NF1 to 17q11.2 by balanced translocation.

Por Ledbetter, D H, Rich, D C, O'Connell, P, Leppert, M, Carey, J C
Publicado em 1989

A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12.

Por Bleyl, S, Nelson, L, Odelberg, S J, Ruttenberg, H D, Otterud, B, Leppert, M, Ward, K
Publicado em 1995

Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.

Por Ptacek, L J, Trimmer, J S, Agnew, W S, Roberts, J W, Petajan, J H, Leppert, M
Publicado em 1991

Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).

Por Chance, P F, Bird, T D, O'Connell, P, Lipe, H, Lalouel, J M, Leppert, M
Publicado em 1990