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Search Results - Robinson, Misi
Search Results - Robinson, Misi
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Natural history of dilated cardiomyopathy due to lamin A/C gene mutations
by
Taylor, Matthew R.G
,
Fain, Pamela R
,
Sinagra, Gianfranco
,
Robinson, Misi L
,
Robertson, Alastair D
,
Carniel, Elisa
,
Di Lenarda, Andrea
,
Bohlmeyer, Teresa J
,
Ferguson, Debra A
,
Brodsky, Gary L
,
Boucek, Mark M
,
Lascor, Jean
,
Moss, Andrew C
,
Li, Wai-Lun P
,
Stetler, Gary L
,
Muntoni, Francesco
,
Bristow, Michael R
,
Mestroni, Luisa
Published in
Journal of the American College of Cardiology
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Genomic Organization and Partial Duplication of the Human α7 Neuronal Nicotinic Acetylcholine Receptor Gene (CHRNA7)
by
Gault, Judith
,
Robinson, Misi
,
Berger, Ralph
,
Drebing, Carla
,
Logel, Judith
,
Hopkins, Jan
,
Moore, Ted
,
Jacobs, Suzette
,
Meriwether, Jennifer
,
Choi, Mun Jun
,
Kim, Eun Jung
,
Walton, Katy
,
Buiting, Karin
,
Davis, Ashley
,
Breese, Charles
,
Freedman, Robert
,
Leonard, Sherry
Published in
Genomics (San Diego, Calif.)
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Detection of ?-galactosidase a mutations causing fabry disease by denaturing high performance liquid chromatography
by
Shabbeer, Junaid
,
Robinson, Misi
,
Desnick, Robert J.
Published in
Human mutation
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Analysis of Genetic Variations of Lamin A/C Gene (LMNA) by Denaturing High-Performance Liquid Chromatography
by
Taylor, Matthew R.G.
,
Robinson, Misi L.
,
Mestroni, Luisa
Published in
SLAS discovery
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Detection of α-galactosidase a mutations causing fabry disease by denaturing high performance liquid chromatography
by
Shabbeer, Junaid
,
Robinson, Misi
,
Desnick, Robert J.
Published in
Human mutation
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Chromosome 3p14 Homozygous Deletions and Sequence Analysis of FRA3B
by
Boldog, Ferenc
,
Gemmill, Robert M.
,
West, James
,
Robinson, Misi
,
Robinson, Linda
,
Li, Efang
,
Roche, Joelle
,
Todd, Sean
,
Waggoner, Barbara
,
Lundstrom, Ron
,
Jacobson, Jan
,
Mullokandov, Michael R.
,
Klinger, Harold
,
Drabkin, Harry A.
Published in
Human molecular genetics
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Further investigation of a chromosome 15 locus in schizophrenia: Analysis of affected sibpairs from the NIMH genetics initiative
by
Leonard, Sherry
,
Gault, Judith
,
Moore, Theodore
,
Hopkins, Jan
,
Robinson, Misi
,
Olincy, Ann
,
Adler, Lawrence E.
,
Cloninger, C. Robert
,
Kaufmann, Charles A.
,
Tsuang, Ming T.
,
Faraone, Stephen V.
,
Malaspina, Dolores
,
Svrakic, Dragan M.
,
Freedman, Robert
Published in
American journal of medical genetics
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ETO and AML1 phosphoproteins are expressed in CD34+ hematopoietic progenitors: implications for t(8;21) leukemogenesis and monitoring residual disease
by
Erickson, PF
,
Dessev, G
,
Lasher, RS
,
Philips, G
,
Robinson, M
,
Drabkin, HA
Published in
Blood
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The ETO portion of acute myeloid leukemia t(8;21) fusion transcript encodes a highly evolutionarily conserved, putative transcription factor
by
ERICKSON, P. F
,
ROBINSON, M
,
OWENS, G
,
DRABKIN, H. A
Published in
Cancer research (Chicago, Ill.)
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A novel γ subunit of the GABA A receptor identified using the polymerase chain reaction
by
Wilson-Shaw, Donna
,
Robinson, Misi
,
Gambarana, Carla
,
Siegel, Ruth E.
,
Sikela, James M.
Published in
FEBS letters
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A novel γ subunit of the GABAA receptor identified using the polymerase chain reaction
by
Wilson-Shaw, Donna
,
Robinson, Misi
,
Gambarana, Carla
,
Siegel, Ruth E.
,
Sikela, James M.
Published in
FEBS letters
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