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Homozygotes for Huntington's disease.
Published in:
Nature, 1987, v. 326, n. 6109, p. 194, doi. 10.1038/326194a0
By:
- Wexler, Nancy S.;
- Young, Anne B.;
- Tanzi, Rudolph E.;
- Travers, Helen;
- Starosta-Rubinstein, Simon;
- Penney, John B.;
- Snodgrass, S. Robert;
- Shoulson, Ira;
- Gomez, Fidela;
- Arroyo, Maria A. Ramos;
- Penchaszadeh, Graciela K.;
- Moreno, Humberto;
- Gibbons, Kerin;
- Faryniarz, Ann;
- Hobbs, Wendy;
- Anderson, Mary Anne;
- Bonilla, Ernesto;
- Conneally, P. Michael;
- Gusella, James F.
Publication type:
Article
Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues.
Published in:
Annals of Neurology, 1997, v. 42, n. 1, p. 41, doi. 10.1002/ana.410420109
By:
- Wang, Ching H.;
- Carter, Todd A.;
- Das, Kamna;
- Xu, Jin;
- Ross, Barbara M.;
- Penchaszadeh, Graciela K.;
- Gilliam, T. Conrad
Publication type:
Article
Association between lipoprotein lipase (LPL) gene and blood lipids: A common variant for a common trait?
Published in:
Genetic Epidemiology, 2003, v. 24, n. 4, p. 309, doi. 10.1002/gepi.10229
By:
- Alfredo Morabia;
- Eftihia Cayanis;
- Michael C. Costanza;
- Barbara M. Ross;
- Martine S. Bernstein;
- Maria Sol Flaherty;
- Gabriela B. Alvin;
- Kamna Das;
- Michael A. Morris;
- Graciela K. Penchaszadeh;
- Peizen Zhang;
- T. Conrad Gilliam
Publication type:
Article
A Multicopy Transcription-Repair Gene, BTF2p44, Maps to the SMA Region and Demonstrates SMA Associated Deletions.
Published in:
Human Molecular Genetics, 1997, v. 6, n. 2, p. 229, doi. 10.1093/hmg/6.2.229
By:
- Carter, Todd A.;
- Bönnemann, Carsten G.;
- Wang, Ching H.;
- Obici, Silvana;
- Parano, Enrico;
- De Fatima Bonaldo, Maria;
- Ross, Barbara M.;
- Penchaszadeh, Graciela K.;
- Mackenzie, Alex;
- Soares, Marcelo Bento;
- Kunkel, Louis M.;
- Gilliam, T. Conrad
Publication type:
Article
Characterization of Survival Motor Neuron (SMNT) Gene Deletions in Asymptomatic Carriers of Spinal Muscular Atrophy.
Published in:
Human Molecular Genetics, 1996, v. 5, n. 3, p. 359, doi. 10.1093/hmg/5.3.359
By:
- Wang, Ching H.;
- Xu, Jin;
- Carter, Todd A.;
- Ross, Barbara M.;
- Dominski, Mary K.;
- Bellcross, Cecelia A.;
- Penchaszadeh, Graciela K.;
- Munsat, Theodore L.;
- Conrad Gilliam, T.
Publication type:
Article

Found: 5

Homozygotes for Huntington's disease.

Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues.

Association between lipoprotein lipase (LPL) gene and blood lipids: A common variant for a common trait?

A Multicopy Transcription-Repair Gene, BTF2p44, Maps to the SMA Region and Demonstrates SMA Associated Deletions.

Characterization of Survival Motor Neuron (SMNT) Gene Deletions in Asymptomatic Carriers of Spinal Muscular Atrophy.