Search research articles
Contact Us
Filters
Showing results (321-330 of 586) with videos related to
Page
of 59
Sort By:
Journal of Medical Case Reports
|
August 5, 2010
Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case report
Joaquín Fernández-Toral, Laura Rodríguez, Ana Plasencia, et al.
Molecular Cytogenetics
|
March 17, 2009
Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation
Bernd Auber, Verena Bruemmer, Barbara Zoll, et al.
Experimental and Therapeutic Medicine
|
March 27, 2014
Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature
Emmanouil Manolakos, Annalisa Vetro, Antonios Garas, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
March 29, 2014
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature
Stavros Sifakis, Makarios Eleftheriades, Dimitra Kappou, et al.
Molecular Genetics & Genomic Medicine
|
January 15, 2022
Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family
Abdulsamad Wafa, Belal Ali, Faten Moassass, et al.
Genes
|
March 28, 2024
Genome and Epigenome Disorders and Male Infertility: Feedback from 15 Years of Clinical and Research Experience
Debbie Montjean, Marion Beaumont, Abdelhafid Natiq, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
September 21, 2014
BAC-probes applied for characterization of fragile sites (FS)
Kristin Mrasek, Kathleen Wilhelm, Luciana G Quintana, et al.
BMC Genomics
|
November 16, 2018
Evidence for a Robertsonian fusion in Solea senegalensis (Kaup, 1858) revealed by zoo-FISH and comparative genome analysis
Aglaya García-Angulo, Manuel A Merlo, Silvia Portela-Bens, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
March 8, 2012
Microdeletion and microduplication syndromes
Anja Weise, Kristin Mrasek, Elisabeth Klein, et al.
Prenatal Diagnosis
|
May 29, 2010
A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth
Ioannis Papoulidis, Emmanouil Manolakos, Elisavet Siomou, et al.
Page
of 59
Search research articles
Search
Showing results (321-330 of 586) with videos related to
Sort By:
Page
of 59
Journal of Medical Case Reports
|
August 5, 2010
Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case report
Joaquín Fernández-Toral, Laura Rodríguez, Ana Plasencia, et al.
Molecular Cytogenetics
|
March 17, 2009
Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation
Bernd Auber, Verena Bruemmer, Barbara Zoll, et al.
Experimental and Therapeutic Medicine
|
March 27, 2014
Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature
Emmanouil Manolakos, Annalisa Vetro, Antonios Garas, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
March 29, 2014
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature
Stavros Sifakis, Makarios Eleftheriades, Dimitra Kappou, et al.
Molecular Genetics & Genomic Medicine
|
January 15, 2022
Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family
Abdulsamad Wafa, Belal Ali, Faten Moassass, et al.
Genes
|
March 28, 2024
Genome and Epigenome Disorders and Male Infertility: Feedback from 15 Years of Clinical and Research Experience
Debbie Montjean, Marion Beaumont, Abdelhafid Natiq, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
September 21, 2014
BAC-probes applied for characterization of fragile sites (FS)
Kristin Mrasek, Kathleen Wilhelm, Luciana G Quintana, et al.
BMC Genomics
|
November 16, 2018
Evidence for a Robertsonian fusion in Solea senegalensis (Kaup, 1858) revealed by zoo-FISH and comparative genome analysis
Aglaya García-Angulo, Manuel A Merlo, Silvia Portela-Bens, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
March 8, 2012
Microdeletion and microduplication syndromes
Anja Weise, Kristin Mrasek, Elisabeth Klein, et al.
Prenatal Diagnosis
|
May 29, 2010
A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth
Ioannis Papoulidis, Emmanouil Manolakos, Elisavet Siomou, et al.
Page
of 59