| | Title | Authors / Editors | Date |
|
unige:643 |
Genomic determinants of the efficiency of internal ribosomal entry sites of viral and cellular origin |
Kazadi, Kayole; Loeuillet, Corinne; Deutsch, Samuel; Ciuffi, Angela; ... Telenti, Amalio |
2008 |
|
unige:2034 |
Contribution of gender-specific genetic factors to osteoporosis risk |
Karasik, D.; Ferrari, Serge Livio |
2008 |
|
unige:8632 |
Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1 |
Beiraghi, Soraya; Nath, S. K.; Gaines, Matthew; Mandhyan, D. D.; ... Radhakrishna, Uppala |
2007 |
|
unige:8740 |
Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation |
Everman, D. B.; Morgan, C. T.; Lyle, Robert; Laughridge, M. E.; ... Schwartz, C. E. |
2006 |
|
unige:8920 |
Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis |
Naveed, Mohammed; Al-Ali, M. T.; Murthy, S. K.; Al-Hajali, Sarah; ... Radhakrishna, Uppala |
2006 |
|
unige:8980 |
Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34 |
Radhakrishna, Uppala; Ratnamala, Uppala; Gaines, Mathew; Beiraghi, Soraya; ... Nath, S. K. |
2006 |
|
unige:9094 |
A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein |
Wattenhofer, Marie; Sahin-Calapoglu, Nilufer; Andreasen, Ditte; Kalay, Ersan; ... Antonarakis, Stylianos |
2005 |
|
unige:11376 |
Identification of 2 major loci linked to autoimmune hemolytic anemia in NZB mice |
Kikuchi, Shuichi; Amano, Hirofumi; Amano, Eri; Fossati-Jimack, Liliane; ... Izui, Shozo |
2005 |
|
unige:7435 |
Structure of Pseudomonas aeruginosa populations analyzed by single nucleotide polymorphism and pulsed-field gel electrophoresis genotyping |
Morales, Gracia; Wiehlmann, Lutz; Gudowius, Peter; Van Delden, Christian; ... Rojo, Fernando |
2004 |
|
unige:11551 |
A novel locus regulates both retroviral glycoprotein 70 and anti-glycoprotein 70 antibody production in New Zealand mice when crossed with BALB/c |
Rigby, R. J.; Rozzo, S. J.; Gill, Herpreet; Fernandez-Hart, Timothy; ... Vyse, T. J. |
2004 |
|
unige:11293 |
Dissection of BXSB lupus phenotype using mice congenic for chromosome 1 demonstrates that separate intervals direct different aspects of disease |
Haywood, M. E.; Rogers, N. J.; Rose, S. J.; Boyle, Joseph; ... Morley, B. J. |
2004 |
|
unige:8900 |
In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis |
Michaud, Joelle; Wu, Feng; Osato, Motomi; Cottles, G. M.; ... Scott, Hamish Steele |
2002 |
|
unige:8873 |
Patterns of meiotic recombination on the long arm of human chromosome 21 |
Lynn, A.; Kashuk, C.; Petersen, M. B.; Bailey, J. A.; ... Chakravarti, A. |
2000 |
|
unige:8974 |
Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes |
Pulver, A. E.; Mulle, J.; Nestadt, G.; Swartz, K. L.; ... McGrath, J. A. |
2000 |
|
unige:8639 |
Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region |
Berry, A.; Scott, Hamish Steele; Kudoh, J.; Talior, I.; ... Bonne-Tamir, B. |
2000 |
|
unige:8649 |
Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity |
Blouin, Jean-Louis; Meeks, M.; Radhakrishna, U.; Sainsbury, A.; ... Antonarakis, Stylianos |
2000 |
|
unige:8698 |
No evidence for linkage between schizophrenia and markers at chromosome 15q13-14 |
Curtis, L.; Blouin, Jean-Louis; Radhakrishna, U.; Gehrig, Corinne; ... Antonarakis, Stylianos |
1999 |
|
unige:8605 |
Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21 |
Antonarakis, Stylianos; Blouin, Jean-Louis; Lasseter, V. K.; Gehrig, Corinne; ... Pulver, A. E. |
1999 |
|
unige:8964 |
APECED: a monogenic autoimmune disease providing new clues to self-tolerance |
Peterson, P.; Nagamine, K.; Scott, Hamish Steele; Heino, M.; ... Krohn, K. J. |
1998 |
|
unige:8600 |
10 years of Genomics, chromosome 21, and Down syndrome |
Antonarakis, Stylianos |
1998 |
Linkage (genetics)
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