| | Title | Authors / Editors | Date |
|
unige:44197 |
Genetic alterations of c-myc, c-erbB-2, and c-Ha-ras protooncogenes and clinical associations in human breast carcinomas |
Garcia, Irène; Dietrich, P Y; Aapro, M; Vauthier, G; ... Engel, E |
1989 |
|
unige:143390 |
Immunogenotyping with antigen receptor gene probes as a diagnostic tool in childhood acute lymphoblastic leukaemia |
Fey, Martin F.; Tobler, Andreas; Stadelmann, Barbara; Hirt, Andreas; ... Wagner, Hans-Peter |
1990 |
|
unige:135904 |
Effect of Rearrangements and Duplications of the Cys-His Motifs of Rous Sarcoma Virus Nucleocapsid Protein |
Bowles, Neil Edward; Damay, Pascal; Spahr, Pierre-François |
1993 |
|
unige:9130 |
Molecular etiology of factor VIII deficiency in hemophilia A |
Antonarakis, Stylianos; Kazazian, H. H.; Gitschier, J.; Hutter, P.; ... Morris, Michael Andréw |
1995 |
|
unige:9131 |
Molecular etiology of factor VIII deficiency in hemophilia A |
Antonarakis, Stylianos; Kazazian, H. H.; Tuddenham, E. G. |
1995 |
|
unige:8599 |
Molecular genetics of coagulation factor VIII gene and haemophilia A |
Antonarakis, Stylianos |
1998 |
|
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:4592 |
Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome |
Mehenni, Hamid; Resta, Nicoletta; Guanti, Ginevra; Mota-Vieira, Louisa; ... Picard, Didier |
2007 |
|
unige:43968 |
NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects |
Lu, Weining; Quintero-Rivera, Fabiola; Fan, Yanli; Alkuraya, Fowzan S; ... Maas, Richard L |
2007 |
|
unige:9219 |
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes |
Mefford, H. C. |
2008 |
Gene rearrangement
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