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Cancer Genetics and Cytogenetics
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October 24, 2001
CGH analysis of secondary genetic changes in Ewing tumors: correlation with metastatic disease in a series of 43 cases
S Brisset, G Schleiermacher, M Peter, et al.
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
|
March 3, 2007
Pure and complete trisomy 18p due to a supernumerary marker chromosome associated with moderate mental retardation
P Mabboux, S Brisset, A Aboura, et al.
Prenatal Diagnosis
|
November 25, 2003
Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15
A Coulomb L'Herminé, A Aboura, S Brisset, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 15, 2008
[Evaluation of the third trimester amniocentesis for fetal karyotyping in women with fear of pregnancy loss]
O Picone, F Fuchs, M-V Sénat, et al.
American Journal of Medical Genetics. Part A
|
October 6, 2006
Terminal 14q32.33 deletion: genotype-phenotype correlation
M-L Maurin, S Brisset, M Le Lorc'h, 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 inversion
M-L Maurin, P Labrune, S Brisset, et al.
Human Reproduction (Oxford, England)
|
April 23, 2005
Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: case report
S Brisset, V Izard, M Misrahi, et al.
American Journal of Medical Genetics
|
November 29, 2002
Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature
S Brisset, G Joly, C Ozilou, et al.
American Journal of Medical Genetics. Part A
|
January 27, 2010
Chromosomal breakpoints characterization of two supernumerary ring chromosomes 20
N Guediche, S Brisset, J-J Benichou, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Cancer Genetics and Cytogenetics
|
October 24, 2001
CGH analysis of secondary genetic changes in Ewing tumors: correlation with metastatic disease in a series of 43 cases
S Brisset, G Schleiermacher, M Peter, et al.
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
|
March 3, 2007
Pure and complete trisomy 18p due to a supernumerary marker chromosome associated with moderate mental retardation
P Mabboux, S Brisset, A Aboura, et al.
Prenatal Diagnosis
|
November 25, 2003
Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15
A Coulomb L'Herminé, A Aboura, S Brisset, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 15, 2008
[Evaluation of the third trimester amniocentesis for fetal karyotyping in women with fear of pregnancy loss]
O Picone, F Fuchs, M-V Sénat, et al.
American Journal of Medical Genetics. Part A
|
October 6, 2006
Terminal 14q32.33 deletion: genotype-phenotype correlation
M-L Maurin, S Brisset, M Le Lorc'h, 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 inversion
M-L Maurin, P Labrune, S Brisset, et al.
Human Reproduction (Oxford, England)
|
April 23, 2005
Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: case report
S Brisset, V Izard, M Misrahi, et al.
American Journal of Medical Genetics
|
November 29, 2002
Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature
S Brisset, G Joly, C Ozilou, et al.
American Journal of Medical Genetics. Part A
|
January 27, 2010
Chromosomal breakpoints characterization of two supernumerary ring chromosomes 20
N Guediche, S Brisset, J-J Benichou, et al.
Page
of 2