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Molecular Genetics & Genomic Medicine
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December 20, 2018
Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception?
Nehir Edibe Kurtas, Luciano Xumerle, Ursula Giussani, et al.
Journal of Assisted Reproduction and Genetics
|
May 14, 2020
Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives
Wafa Slimani, Afef Jelloul, Ahmed Al-Rikabi, et al.
European Journal of Human Genetics : EJHG
|
October 23, 2003
Karyotyping of human synaptonemal complexes by cenM-FISH
Maria Oliver-Bonet, Thomas Liehr, Angela Nietzel, et al.
Scientific Reports
|
September 2, 2024
Satellite DNAs and the evolution of the multiple X<sub>1</sub>X<sub>2</sub>Y sex chromosomes in the wolf fish Hoplias malabaricus (Teleostei; Characiformes)
Gustavo Akira Toma, Alexandr Sember, Caio Augusto Gomes Goes, et al.
Molecular Syndromology
|
October 3, 2024
<i>De novo</i> <i>AHDC1</i> Deletions Identified by Genome Sequencing in Two Individuals with Xia-Gibbs Syndrome
Miriam Bertrand, Gulalai Shah, Brent S Pedersen, et al.
Cancer Genetics and Cytogenetics
|
February 2, 2010
Molecular cytogenetic studies characterize a near-triploid complex karyotype in a child with acute lymphoblastic leukemia
Hasmik Mkrtchyan, Daniela Ribeiro Garcia Ney, Eliane Soares de Ventura, et al.
Acta Haematologica
|
July 4, 2015
A Novel Three-Way Variant t(8;13;21)(q22;q33;q22) in a Child with Acute Myeloid Leukemia with RUNX1/RUNX1T1 : The Contribution of Molecular Approaches for Revealing t(8;21) Variants
Roberto R Capela de Matos, Amanda F De Figueiredo, Thomas Liehr, et al.
European Journal of Human Genetics : EJHG
|
August 8, 2008
Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions
Samarth Bhatt, Kamran Moradkhani, Kristin Mrasek, et al.
Journal of Applied Genetics
|
March 26, 2011
Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances
Joana Barbosa Melo, Liesbeth Backx, Joris R Vermeesch, et al.
Comparative Cytogenetics
|
May 7, 2021
Comparative study of four <i>Mystus</i> species (Bagridae, Siluriformes) from Thailand: insights into their karyotypic diversity
Pun Yeesin, Phichaya Buasriyot, Sukhonthip Ditcharoen, et al.
Page
of 59
Search research articles
Search
Showing results (411-420 of 586) with videos related to
Sort By:
Page
of 59
Molecular Genetics & Genomic Medicine
|
December 20, 2018
Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception?
Nehir Edibe Kurtas, Luciano Xumerle, Ursula Giussani, et al.
Journal of Assisted Reproduction and Genetics
|
May 14, 2020
Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives
Wafa Slimani, Afef Jelloul, Ahmed Al-Rikabi, et al.
European Journal of Human Genetics : EJHG
|
October 23, 2003
Karyotyping of human synaptonemal complexes by cenM-FISH
Maria Oliver-Bonet, Thomas Liehr, Angela Nietzel, et al.
Scientific Reports
|
September 2, 2024
Satellite DNAs and the evolution of the multiple X<sub>1</sub>X<sub>2</sub>Y sex chromosomes in the wolf fish Hoplias malabaricus (Teleostei; Characiformes)
Gustavo Akira Toma, Alexandr Sember, Caio Augusto Gomes Goes, et al.
Molecular Syndromology
|
October 3, 2024
<i>De novo</i> <i>AHDC1</i> Deletions Identified by Genome Sequencing in Two Individuals with Xia-Gibbs Syndrome
Miriam Bertrand, Gulalai Shah, Brent S Pedersen, et al.
Cancer Genetics and Cytogenetics
|
February 2, 2010
Molecular cytogenetic studies characterize a near-triploid complex karyotype in a child with acute lymphoblastic leukemia
Hasmik Mkrtchyan, Daniela Ribeiro Garcia Ney, Eliane Soares de Ventura, et al.
Acta Haematologica
|
July 4, 2015
A Novel Three-Way Variant t(8;13;21)(q22;q33;q22) in a Child with Acute Myeloid Leukemia with RUNX1/RUNX1T1 : The Contribution of Molecular Approaches for Revealing t(8;21) Variants
Roberto R Capela de Matos, Amanda F De Figueiredo, Thomas Liehr, et al.
European Journal of Human Genetics : EJHG
|
August 8, 2008
Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions
Samarth Bhatt, Kamran Moradkhani, Kristin Mrasek, et al.
Journal of Applied Genetics
|
March 26, 2011
Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances
Joana Barbosa Melo, Liesbeth Backx, Joris R Vermeesch, et al.
Comparative Cytogenetics
|
May 7, 2021
Comparative study of four <i>Mystus</i> species (Bagridae, Siluriformes) from Thailand: insights into their karyotypic diversity
Pun Yeesin, Phichaya Buasriyot, Sukhonthip Ditcharoen, et al.
Page
of 59