caa a22 4500 467986533 CHVBK 20180323112533.0 cr unu---uuuuu 170328e19901201xx s 000 0 eng 10.1007/BF00197694 doi (NATIONALLICENCE)springer-10.1007/BF00197694 The human MyoD1 (MYF3) gene maps on the short arm of chromosome 11 but is not associated with the WAGR locus or the region for the Beckwith-Wiedemann syndrome [Elektronische Daten] [M. Gessler, H. Hameister, I. Henry, C. Junien, T. Braun, H. Arnold] Summary: The human gene encoding the myogenic determination factor myf3 (mouse MyoD1) has been mapped to the short arm of chromosome 11. Analysis of several somatic cell hybrids containing various derivatives with deletions or translocations revealed that the human MyoD (MYF3) gene is not associated with the WAGR locus at chromosomal band 11p13 nor with the loss of the heterozygosity region at 11p15.5 related to the Beckwith-Wiedemann syndrome. Subregional mapping by in situ hybridization with an myf3 specific probe shows that the gene resides at the chromosomal band 11p14, possibly at 11pl4.3. Springer-Verlag, 1990 Gessler M. Genetics Division, The Children's Hospital, 02115, Boston, MA, USA aut Hameister H. Abteilung Klinische Genetik der Universität, Albert-Einstein-Allee 11, W-7900, Ulm, Germany aut Henry I. INSERM, Chateau de Longchamp, F-75016, Paris, France aut Junien C. INSERM, Chateau de Longchamp, F-75016, Paris, France aut Braun T. Abteilung Allgemeine Toxikologie, Universitätskrankenhaus Eppendorf, Grindelallee 117, W-2000, Hamburg 13, Germany aut Arnold H. Abteilung Allgemeine Toxikologie, Universitätskrankenhaus Eppendorf, Grindelallee 117, W-2000, Hamburg 13, Germany aut Human Genetics Springer-Verlag 86/2(1990-12-01), 135-138 0340-6717 86:2<135 1990 86 439 https://doi.org/10.1007/BF00197694 text/html Onlinezugriff via DOI 1 research-article jats NATIONALLICENCE 856 40 https://doi.org/10.1007/BF00197694 text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Gessler M. Genetics Division, The Children's Hospital, 02115, Boston, MA, USA aut NATIONALLICENCE 700 1- Hameister H. Abteilung Klinische Genetik der Universität, Albert-Einstein-Allee 11, W-7900, Ulm, Germany aut NATIONALLICENCE 700 1- Henry I. INSERM, Chateau de Longchamp, F-75016, Paris, France aut NATIONALLICENCE 700 1- Junien C. INSERM, Chateau de Longchamp, F-75016, Paris, France aut NATIONALLICENCE 700 1- Braun T. Abteilung Allgemeine Toxikologie, Universitätskrankenhaus Eppendorf, Grindelallee 117, W-2000, Hamburg 13, Germany aut NATIONALLICENCE 700 1- Arnold H. Abteilung Allgemeine Toxikologie, Universitätskrankenhaus Eppendorf, Grindelallee 117, W-2000, Hamburg 13, Germany aut NATIONALLICENCE 773 0- Human Genetics Springer-Verlag 86/2(1990-12-01), 135-138 0340-6717 86:2<135 1990 86 439 Metadata rights reserved Springer special CC-BY-NC licence nationallicence BK010053 XK010053 XK010000 NATIONALLICENCE NATIONALLICENCE NL-springer