Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene

L Toffolatti, B Cardazzo, C Nobile, GA Danieli… - Genomics, 2002 - Elsevier
The region of the dystrophin gene containing introns 45–50 is characterized by a high rate of
recombination events that give rise to large deletions causing dystrophinopathy. The …

[引用][C] Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene

L TOFFOLATTI - Genomics, 2002 - cir.nii.ac.jp
Investigating the mechanism of chromosomal deletion : characterization of 39 deletion
breakpoints in introns 47 and 48 of the human dystrophin gene | CiNii Research CiNii 国立 …

[PDF][PDF] Investigating the Mechanism of Chromosomal Deletion: Characterization of 39 Deletion Breakpoints in Introns 47 and 48 of the Human Dystrophin Gene

L Toffolatti, B Cardazzo, C Nobile, GA Danieli… - GENOMICS, 2002 - researchgate.net
The region of the dystrophin gene containing introns 45–50 is characterized by a high rate of
recombination events that give rise to large deletions causing dystrophinopathy. The …

Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene.

L Toffolatti, B Cardazzo, C Nobile, GA Danieli… - Genomics, 2002 - europepmc.org
The region of the dystrophin gene containing introns 45-50 is characterized by a high rate of
recombination events that give rise to large deletions causing dystrophinopathy. The …

Investigating the mechanism of chromosomal deletion: Characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene

L Toffolatti, B Cardazzo, C Nobile, G Danieli… - GENOMICS, 2002 - sfera.unife.it
The region of the dystrophin gene containing introns 45-50 is characterized by a high rate of
recombination events that give rise to large deletions causing dystrophinopathy. The …

Investigating the Mechanism of Chromosomal Deletion: Characterization of 39 Deletion Breakpoints in Introns 47 and 48 of the Human Dystrophin Gene

L Toffolatti, B Cardazzo, C Nobile, GA Danieli… - Genomics, 2002 - elibrary.ru
The region of the dystrophin gene containing introns 45-50 is characterized by a high rate of
recombination events that give rise to large deletions causing dystrophinopathy. The …

Investigating the Mechanism of Chromosomal Deletion: Characterization of 39 Deletion Breakpoints in Introns 47 and 48 of the Human Dystrophin Gene

L Toffolatti, B Cardazzo, C Nobile, GA Danieli… - Genomics, 2002 - infona.pl
The region of the dystrophin gene containing introns 45-50 is characterized by a high rate of
recombination events that give rise to large deletions causing dystrophinopathy. The …

Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene

L Toffolatti, B Cardazzo, C Nobile, GA Danieli… - …, 2002 - pubmed.ncbi.nlm.nih.gov
The region of the dystrophin gene containing introns 45-50 is characterized by a high rate of
recombination events that give rise to large deletions causing dystrophinopathy. The …

Investigating the mechanism of chromosomal deletion: Characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene

L Toffolatti, B Cardazzo, C Nobile, G Danieli… - GENOMICS, 2002 - research.unipd.it
The region of the dystrophin gene containing introns 45-50 is characterized by a high rate of
recombination events that give rise to large deletions causing dystrophinopathy. The …

[引用][C] Investigating the mechanism of chromosomal deletion: Characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene

L TOFFOLATTI, B CARDAZZO… - … (San Diego, Calif.), 2002 - pascal-francis.inist.fr
Investigating the mechanism of chromosomal deletion: Characterization of 39 deletion
breakpoints in introns 47 and 48 of the human dystrophin gene CNRS Inist Pascal-Francis …