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

Bằng Leppert, M, Kolakofsky, D
Được phát hành 1980

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

Bằng Leppert, M, Kolakofsky, D
Được phát hành 1978

Cytogenetic and molecular analysis of sex-chromosome monosomy.

Bằng Hassold, T, Benham, F, Leppert, M
Được phát hành 1988

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

Bằng Hassold, T, Kumlin, E, Takaesu, N, Leppert, M
Được phát hành 1985

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

Bằng Litt, M, Litt, R, Ballard, L, Leppert, M
Được phát hành 1989

Cytogenetic and molecular studies of trisomy 13.

Bằng Hassold, T, Jacobs, P A, Leppert, M, Sheldon, M
Được phát hành 1987

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

Bằng Hasstedt, S J, Hoffman, M, Leppert, M F, Elbein, S C
Được phát hành 1997

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

Bằng Spirio, L., Joslyn, G., Nelson, L., Leppert, M., White, R.
Được phát hành 1991

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

Bằng Heath, H, Jackson, C E, Otterud, B, Leppert, M F
Được phát hành 1993

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

Bằng German, J, Roe, A M, Leppert, M F, Ellis, N A
Được phát hành 1994

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

Bằng Ptacek, L J, Tyler, F, Trimmer, J S, Agnew, W S, Leppert, M
Được phát hành 1991

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

Bằng Naumova, A K, Leppert, M, Barker, D F, Morgan, K, Sapienza, C
Được phát hành 1998

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

Bằng Spirio, L, Nelson, L, Ward, K, Burt, R, White, R, Leppert, M
Được phát hành 1993

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

Bằng Keating, M, Dunn, C, Atkinson, D, Timothy, K, Vincent, G M, Leppert, M
Được phát hành 1991

Characterization of a human 'midisatellite' sequence.

Bằng Nakamura, Y, Julier, C, Wolff, R, Holm, T, O'Connell, P, Leppert, M, White, R
Được phát hành 1987

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

Bằng Dean, M., Stewart, C., Perry, A., Stauffer, D., Otterud, B., White, R., Leppert, M.
Được phát hành 1991

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

Bằng Ledbetter, D H, Rich, D C, O'Connell, P, Leppert, M, Carey, J C
Được phát hành 1989

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

Bằng Bleyl, S, Nelson, L, Odelberg, S J, Ruttenberg, H D, Otterud, B, Leppert, M, Ward, K
Được phát hành 1995

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

Bằng Ptacek, L J, Trimmer, J S, Agnew, W S, Roberts, J W, Petajan, J H, Leppert, M
Được phát hành 1991

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

Bằng Chance, P F, Bird, T D, O'Connell, P, Lipe, H, Lalouel, J M, Leppert, M
Được phát hành 1990