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M-L Maurin

Showing results (1-10 of 4) with videos related to

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Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|December 28, 2007
[Risk of missed diagnosis of 22q11.2 deletion in a fetal cardiac conotruncal malformation when another chromosomal abnormality is detected]O Picone, S Brisset, M-V Senat, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Molecular cytogenetic characterization of a 4p15.1-pter duplication and a 4q35.1-qter deletion in a recombinant of chromosome 4 pericentric inversionM-L Maurin, P Labrune, S Brisset, et al.
American Journal of Medical Genetics. Part A|October 6, 2006
Terminal 14q32.33 deletion: genotype-phenotype correlationM-L Maurin, S Brisset, M Le Lorc'h, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Chromosomal breakpoints characterization of two supernumerary ring chromosomes 20N Guediche, S Brisset, J-J Benichou, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|December 28, 2007
[Risk of missed diagnosis of 22q11.2 deletion in a fetal cardiac conotruncal malformation when another chromosomal abnormality is detected]O Picone, S Brisset, M-V Senat, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Molecular cytogenetic characterization of a 4p15.1-pter duplication and a 4q35.1-qter deletion in a recombinant of chromosome 4 pericentric inversionM-L Maurin, P Labrune, S Brisset, et al.
American Journal of Medical Genetics. Part A|October 6, 2006
Terminal 14q32.33 deletion: genotype-phenotype correlationM-L Maurin, S Brisset, M Le Lorc'h, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Chromosomal breakpoints characterization of two supernumerary ring chromosomes 20N Guediche, S Brisset, J-J Benichou, et al.
Pageof 1