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Results: 1-8 |
Results: 8
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds
Authors: Zoghbi, Huda Y. Jodice, Carla Sandkuijl, Lodewijk A. Kwiatkowski, Thomas J. Jr McCall, Alanna E. Huntoon, Sally A. Lulli, Patrizia Spadaro, Maria Litt, Michael Cann, Howard M. Frontali, Marina Terrenato, Luciano
Citation: Y. Zoghbi, Huda et al., The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds, American journal of human genetics , 49-I(1), 1991, pp. 23-30
Assignment of autosomal dominant spinocerebellar ataxia (scal) centromeric to the hla region on the short arm of chromosome 6, using multilocus linkage analysis
Authors: Zoghbi, Huda Y. Sandkuyl, Lodewyk A. Ott, jurg P. Daiger, Stephen Pollack, Marilyn O'Brien, William E Beaudet, Arthur L.
Citation: Y. Zoghbi, Huda et al., Assignment of autosomal dominant spinocerebellar ataxia (scal) centromeric to the hla region on the short arm of chromosome 6, using multilocus linkage analysis, American journal of human genetics , 44(2), 1989, pp. 255-263
X-Chromosome Inactivation Patterns Are Unbalanced and Affect the Phenotypic Outcome in a Mouse Model of Rett Syndrome
Authors: Young, Juan I. Zoghbi, Huda Y.
Citation: I. Young, Juan et Y. Zoghbi, Huda, X-Chromosome Inactivation Patterns Are Unbalanced and Affect the Phenotypic Outcome in a Mouse Model of Rett Syndrome, American journal of human genetics , 74(3), 2004, pp. 511-520
Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6
Authors: Ledley, Fred D. Lumetta, Michele R. Zoghbi, Huda Y. Tuinen, Peter van Ledbetter, Susan A. Ledbetter, David H.
Citation: D. Ledley, Fred et al., Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6, American journal of human genetics , 42(6), 1988, pp. 839-846
Extensive DNA polymorphism at the factor XIlla (FI3A) locus and linkage to HLA
Authors: Zoghbi, Huda Y. Daiger, Stephen P. McCall, Alanna O'Brien, William E. Beaudet, Arthur L.
Citation: Y. Zoghbi, Huda et al., Extensive DNA polymorphism at the factor XIlla (FI3A) locus and linkage to HLA, American journal of human genetics , 42(6), 1988, pp. 877-883
Somatic and Germline Instability of the ATTCT Repeat in Spinocerebellar Ataxia Type 10
Authors: Matsuura, Tohru Fang, Ping Lin, Xi Khajavi, Mehrdad Tsuji, Kuuniko Rasmussen, Astrid Grewal, Raji P. Achari, Madhureeta Alonso, Maria E. Pulst, Stefan M. Zoghbi, Huda Y. Nelson, David L. Roa, Benjamin B. Ashizawa, Tetsuo
Citation: Matsuura, Tohru et al., Somatic and Germline Instability of the ATTCT Repeat in Spinocerebellar Ataxia Type 10, American journal of human genetics , 74(6), 2004, pp. 1216-1224
Rett Syndrome and MeCP2: Linking Epigenetics and Neuronal Function
Authors: Shahbazian, Mona D. Zoghbi, Huda Y.
Citation: D. Shahbazian, Mona et Y. Zoghbi, Huda, Rett Syndrome and MeCP2: Linking Epigenetics and Neuronal Function, American journal of human genetics , 71(6), 2002, pp. 1259-1272
Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26).
Authors: Huang, Tim H-M. Hejtmancik, J. Fielding Edwards, Al Pettigrew, Anjana L. Herrera, Carlos A. Hammond, Holly A. Caskey, C. Thomas Zoghbi, Huda Y. Ledbetter, David H.
Citation: Huang, Tim H-m et al., Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26)., American journal of human genetics , 49-II(5), 1991, pp. 1312-1319
Risultati: 1-8 |