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Methods in Molecular Biology (Clifton, N.J.)
|
August 30, 2025
ISCN and Chromoanagenesis
Martine Doco-Fenzy, Jean-Michel Dupont, Caroline Schluth-Bolard
Analytical Biochemistry
|
September 8, 2004
De novo quantitative bisulfite sequencing using the pyrosequencing technology
Jean-Michel Dupont, Jörg Tost, Hélène Jammes, et al.
European Journal of Medical Genetics
|
October 31, 2006
Pure familial 6q21q22.1 duplication in two generations
Mohammad Pazooki, Aziza Lebbar, Anne Roubergues, et al.
Prenatal Diagnosis
|
February 29, 2008
Optimized criteria for using fluorescence in situ hybridization in the prenatal diagnosis of common aneuploidies
Sandrine Leclercq, Aziza Lebbar, Gilles Grange, et al.
Prenatal Diagnosis
|
July 11, 2008
Maternal serum screening in cases of mosaic and translocation Down syndrome
Sophie Dreux, Camille Olivier, Jean-Michel Dupont, et al.
Journal of Gynecology Obstetrics and Human Reproduction
|
January 15, 2026
Chromosomal abnormalities diagnosed at the chromosomal microarray in pregnancies with isolated high risk of trisomy 21
Helyett Ollivier, Valérie Malan, Raphael Bartin, et al.
Epigenetics
|
July 22, 2011
Methylation of specific CpG sites in the P2 promoter of parathyroid hormone-related protein determines the invasive potential of breast cancer cell lines
Jörg Tost, Hinda Hamzaoui, Florence Busato, et al.
American Journal of Medical Genetics
|
September 5, 2002
Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver-Russell patient
Jean-Michel Dupont, Laurence Cuisset, Maryse Cartigny, et al.
American Journal of Medical Genetics. Part A
|
April 28, 2016
A de novo 10p11.23-p12.1 deletion recapitulates the phenotype observed in WAC mutations and strengthens the role of WAC in intellectual disability and behavior disorders
Fatma Abdelhedi, Laila El Khattabi, Nouha Essid, et al.
American Journal of Medical Genetics. Part A
|
February 12, 2009
Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model
Sandrine Leclercq, Kim Maincent, Françoise Baverel, et al.
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of 5
Search research articles
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Showing results (1-10 of 46) with videos related to
Sort By:
Page
of 5
Methods in Molecular Biology (Clifton, N.J.)
|
August 30, 2025
ISCN and Chromoanagenesis
Martine Doco-Fenzy, Jean-Michel Dupont, Caroline Schluth-Bolard
Analytical Biochemistry
|
September 8, 2004
De novo quantitative bisulfite sequencing using the pyrosequencing technology
Jean-Michel Dupont, Jörg Tost, Hélène Jammes, et al.
European Journal of Medical Genetics
|
October 31, 2006
Pure familial 6q21q22.1 duplication in two generations
Mohammad Pazooki, Aziza Lebbar, Anne Roubergues, et al.
Prenatal Diagnosis
|
February 29, 2008
Optimized criteria for using fluorescence in situ hybridization in the prenatal diagnosis of common aneuploidies
Sandrine Leclercq, Aziza Lebbar, Gilles Grange, et al.
Prenatal Diagnosis
|
July 11, 2008
Maternal serum screening in cases of mosaic and translocation Down syndrome
Sophie Dreux, Camille Olivier, Jean-Michel Dupont, et al.
Journal of Gynecology Obstetrics and Human Reproduction
|
January 15, 2026
Chromosomal abnormalities diagnosed at the chromosomal microarray in pregnancies with isolated high risk of trisomy 21
Helyett Ollivier, Valérie Malan, Raphael Bartin, et al.
Epigenetics
|
July 22, 2011
Methylation of specific CpG sites in the P2 promoter of parathyroid hormone-related protein determines the invasive potential of breast cancer cell lines
Jörg Tost, Hinda Hamzaoui, Florence Busato, et al.
American Journal of Medical Genetics
|
September 5, 2002
Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver-Russell patient
Jean-Michel Dupont, Laurence Cuisset, Maryse Cartigny, et al.
American Journal of Medical Genetics. Part A
|
April 28, 2016
A de novo 10p11.23-p12.1 deletion recapitulates the phenotype observed in WAC mutations and strengthens the role of WAC in intellectual disability and behavior disorders
Fatma Abdelhedi, Laila El Khattabi, Nouha Essid, et al.
American Journal of Medical Genetics. Part A
|
February 12, 2009
Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model
Sandrine Leclercq, Kim Maincent, Françoise Baverel, et al.
Page
of 5