Show items per page
Elements: 10
Page 1 on 1
 TitleAuthors / EditorsDate
add to browser selection
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes Mefford, H. C. 2008
add to browser selection
Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome Mehenni, Hamid; Resta, Nicoletta; Guanti, Ginevra; Mota-Vieira, Louisa; ... Picard, Didier 2007
add to browser selection
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
add to browser selection
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
add to browser selection
Molecular genetics of coagulation factor VIII gene and haemophilia A Antonarakis, Stylianos 1998
add to browser selection
Molecular etiology of factor VIII deficiency in hemophilia A Antonarakis, Stylianos; Kazazian, H. H.; Gitschier, J.; Hutter, P.; ... Morris, Michael Andréw 1995
add to browser selection
Molecular etiology of factor VIII deficiency in hemophilia A Antonarakis, Stylianos; Kazazian, H. H.; Tuddenham, E. G. 1995
add to browser selection
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
add to browser selection
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
add to browser selection
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