A Clone Contig of 12q24.3 Encompassing the Distal Hereditary Motor Neuropathy Type II Gene

Genomics ◽  
2000 ◽  
Vol 65 (1) ◽  
pp. 34-43 ◽  
Author(s):  
Joy Irobi ◽  
Fadel Tissir ◽  
Peter De Jonghe ◽  
Els De Vriendt ◽  
Christine Van Broeckhoven ◽  
...  
2000 ◽  
Vol 5 (4) ◽  
pp. 242-242
Author(s):  
J Irobi ◽  
F Tissir ◽  
P De Jonghe ◽  
E De Vriendt ◽  
C Van Broeckhoven ◽  
...  

1999 ◽  
Vol 883 (1) ◽  
pp. 60-64 ◽  
Author(s):  
V. TIMMERMAN ◽  
J. BEUTEN ◽  
J. IROBI ◽  
P. De JONGHE ◽  
J.-J. MARTIN ◽  
...  

2019 ◽  
Vol 2 (1) ◽  
pp. 01-03
Author(s):  
Shahin Asadi

Symptoms of DHMN2 usually begin from the age of 10 to the middle of adulthood. Early signs of this disorder include clogging or weakness in the muscles of the toe and the next, the whole leg. The DHMN2 syndrome is caused by the mutation of the HSPB1 gene, which is positioned in the long arm of chromosome 7 as 7q11.23, and the HSPB8 gene, which is based on the long arm of chromosome 12, is 12q24.23.


1999 ◽  
Vol 883 (1) ◽  
pp. 463-465
Author(s):  
JOY IROBI ◽  
VINCENT TIMMERMAN ◽  
PETER De JONGHE ◽  
ELS De VRIENDT ◽  
CHRISTINE VAN BROECKHOVEN ◽  
...  

2000 ◽  
Vol 5 (4) ◽  
pp. 242-242
Author(s):  
J Irobi ◽  
F Tissir ◽  
P De Jonghe ◽  
E De Vriendt ◽  
C Van Broeckhoven ◽  
...  

2002 ◽  
Vol 7 (2) ◽  
pp. 87-95 ◽  
Author(s):  
Joy Irobi ◽  
Eva Nelis ◽  
Kristien Verhoeven ◽  
Els De Vriendt ◽  
Ines Dierick ◽  
...  

1997 ◽  
Vol 223 (1) ◽  
pp. 69-71 ◽  
Author(s):  
Joke Beuten ◽  
Els De Vriendt ◽  
Peter De Jonghe ◽  
Jean-Jacques Martin ◽  
Christine Van Broeckhoven ◽  
...  

2001 ◽  
Vol 65 (6) ◽  
pp. 517-529 ◽  
Author(s):  
J. IROBI ◽  
E. NELIS ◽  
J. MEULEMAN ◽  
K. VENKEN ◽  
P. JONGHE ◽  
...  

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