Ngā hua rapu kaituhi

1

Effect of defective interfering particles on plus- and minus- strand leader RNAs in vesicular stomatitis virus-infected cells. mā Leppert, M, Kolakofsky, D

I whakaputaina 1980

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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2

5' Terminus of defective and nondefective Sendai viral genomes is ppp Ap. mā Leppert, M, Kolakofsky, D

I whakaputaina 1978

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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3

Cytogenetic and molecular analysis of sex-chromosome monosomy. mā Hassold, T, Benham, F, Leppert, M

I whakaputaina 1988

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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4

Determination of the parental origin of sex-chromosome monosomy using restriction fragment length polymorphisms. mā Hassold, T, Kumlin, E, Takaesu, N, Leppert, M

I whakaputaina 1985

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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5

Cytogenetic and molecular studies of trisomy 13. mā Hassold, T, Jacobs, P A, Leppert, M, Sheldon, M

I whakaputaina 1987

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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6

An anonymous single-copy clone, p30-1-60, identifies a frequent RFLP on chromosome 3p [HGM9 no. D3S86]. mā Litt, M, Litt, R, Ballard, L, Leppert, M

I whakaputaina 1989

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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7

Recessive inheritance of obesity in familial non-insulin-dependent diabetes mellitus, and lack of linkage to nine candidate genes. mā Hasstedt, S J, Hoffman, M, Leppert, M F, Elbein, S C

I whakaputaina 1997

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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8

Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity. mā Heath, H, Jackson, C E, Otterud, B, Leppert, M F

I whakaputaina 1993

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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9

A CA repeat 30–70 KB downstream from the adenomatous polyposis coli (APC) gene mā Spirio, L., Joslyn, G., Nelson, L., Leppert, M., White, R.

I whakaputaina 1991

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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10

Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus. mā Ptacek, L J, Tyler, F, Trimmer, J S, Agnew, W S, Leppert, M

I whakaputaina 1991

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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11

Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1. mā German, J, Roe, A M, Leppert, M F, Ellis, N A

I whakaputaina 1994

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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12

Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome. mā Naumova, A K, Leppert, M, Barker, D F, Morgan, K, Sapienza, C

I whakaputaina 1998

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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13

A CA-repeat polymorphism close to the adenomatous polyposis coli (APC) gene offers improved diagnostic testing for familial APC. mā Spirio, L, Nelson, L, Ward, K, Burt, R, White, R, Leppert, M

I whakaputaina 1993

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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14

Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11. mā Keating, M, Dunn, C, Atkinson, D, Timothy, K, Vincent, G M, Leppert, M

I whakaputaina 1991

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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15

Precise localization of NF1 to 17q11.2 by balanced translocation. mā Ledbetter, D H, Rich, D C, O'Connell, P, Leppert, M, Carey, J C

I whakaputaina 1989

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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16

A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12. mā Bleyl, S, Nelson, L, Odelberg, S J, Ruttenberg, H D, Otterud, B, Leppert, M, Ward, K

I whakaputaina 1995

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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17

D7S448 detects a HindIII polymorphism located in the centromere region of chromosome 7 mā Dean, M., Stewart, C., Perry, A., Stauffer, D., Otterud, B., White, R., Leppert, M.

I whakaputaina 1991

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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18

Characterization of a human 'midisatellite' sequence. mā Nakamura, Y, Julier, C, Wolff, R, Holm, T, O'Connell, P, Leppert, M, White, R

I whakaputaina 1987

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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19

Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus. mā Ptacek, L J, Trimmer, J S, Agnew, W S, Roberts, J W, Petajan, J H, Leppert, M

I whakaputaina 1991

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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20

Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I). mā Chance, P F, Bird, T D, O'Connell, P, Lipe, H, Lalouel, J M, Leppert, M

I whakaputaina 1990

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Ngā hua rapu - Leppert, M

Effect of defective interfering particles on plus- and minus- strand leader RNAs in vesicular stomatitis virus-infected cells. mā Leppert, M, Kolakofsky, D

5' Terminus of defective and nondefective Sendai viral genomes is ppp Ap. mā Leppert, M, Kolakofsky, D

Cytogenetic and molecular analysis of sex-chromosome monosomy. mā Hassold, T, Benham, F, Leppert, M

Determination of the parental origin of sex-chromosome monosomy using restriction fragment length polymorphisms. mā Hassold, T, Kumlin, E, Takaesu, N, Leppert, M

Cytogenetic and molecular studies of trisomy 13. mā Hassold, T, Jacobs, P A, Leppert, M, Sheldon, M

An anonymous single-copy clone, p30-1-60, identifies a frequent RFLP on chromosome 3p [HGM9 no. D3S86]. mā Litt, M, Litt, R, Ballard, L, Leppert, M

Recessive inheritance of obesity in familial non-insulin-dependent diabetes mellitus, and lack of linkage to nine candidate genes. mā Hasstedt, S J, Hoffman, M, Leppert, M F, Elbein, S C

Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity. mā Heath, H, Jackson, C E, Otterud, B, Leppert, M F

A CA repeat 30–70 KB downstream from the adenomatous polyposis coli (APC) gene mā Spirio, L., Joslyn, G., Nelson, L., Leppert, M., White, R.

Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus. mā Ptacek, L J, Tyler, F, Trimmer, J S, Agnew, W S, Leppert, M

Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1. mā German, J, Roe, A M, Leppert, M F, Ellis, N A

Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome. mā Naumova, A K, Leppert, M, Barker, D F, Morgan, K, Sapienza, C

A CA-repeat polymorphism close to the adenomatous polyposis coli (APC) gene offers improved diagnostic testing for familial APC. mā Spirio, L, Nelson, L, Ward, K, Burt, R, White, R, Leppert, M

Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11. mā Keating, M, Dunn, C, Atkinson, D, Timothy, K, Vincent, G M, Leppert, M

Precise localization of NF1 to 17q11.2 by balanced translocation. mā Ledbetter, D H, Rich, D C, O'Connell, P, Leppert, M, Carey, J C

A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12. mā Bleyl, S, Nelson, L, Odelberg, S J, Ruttenberg, H D, Otterud, B, Leppert, M, Ward, K

D7S448 detects a HindIII polymorphism located in the centromere region of chromosome 7 mā Dean, M., Stewart, C., Perry, A., Stauffer, D., Otterud, B., White, R., Leppert, M.

Characterization of a human 'midisatellite' sequence. mā Nakamura, Y, Julier, C, Wolff, R, Holm, T, O'Connell, P, Leppert, M, White, R

Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus. mā Ptacek, L J, Trimmer, J S, Agnew, W S, Roberts, J W, Petajan, J H, Leppert, M

Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I). mā Chance, P F, Bird, T D, O'Connell, P, Lipe, H, Lalouel, J M, Leppert, M

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