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Developmental Medicine and Child Neurology
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March 16, 2007
Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3)
Sevim Balci, Aysun Unal, Ozlem Engiz, et al.
Comparative Cytogenetics
|
August 23, 2014
Genomic organization of repetitive DNAs and its implications for male karyotype and the neo-Y chromosome differentiation in Erythrinus erythrinus (Characiformes, Erythrinidae)
Cassia Fernanda Yano, Luiz Antonio Carlos Bertollo, Wagner Franco Molina, et al.
Gene
|
March 1, 2015
A cryptic three-way translocation t(10;19;11)(p12.31;q13.31;q23.3) with a derivative Y-chromosome in an infant with acute myeloblastic leukemia (M5b)
Moneeb A K Othman, Dragana Vujić, Zeljko Zecević, et al.
Journal of Genetics
|
September 21, 2023
Molecular characterization of <i>de novo</i> ring chromosome 21 in a child with seizures, growth retardation, and multiple congenital anomalies
Prafulla S Ambulkar, Thomas Liehr, Manish Jain, et al.
International Journal of Oncology
|
January 17, 2009
Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype
Madeleine Gross, Hasmik Mkrtchyan, Melanie Glaser, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2006
Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomalies
Sevim Balci, Ozlem Engiz, Dilek Aktaş, et al.
International Journal of Molecular Medicine
|
January 5, 2006
Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping and multicolor banding applying murine probes
Constanze Karst, Vladimir Trifonov, Svetlana A Romanenko, et al.
Journal of Pediatric Genetics
|
August 11, 2017
Unusual de novo Partial Trisomy 17p12p11.2 due to Unbalanced Insertion into 5p13.1 in a Severely Affected Boy
Luis Alberto Mendez-Rosado, Araceli Lantigua, Juan Galarza, et al.
Heliyon
|
December 21, 2023
CHD2 pathogenic nonsense variant in a three-generation family with variable phenotype and a paracentric inversion 16: Case report
Eleni Angelopoulou, Athina Theodosiou, Ioannis Papaevripidou, et al.
Frontiers in Genetics
|
March 11, 2024
A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature
Fatima Ouboukss, Zhour El Amrani, Hicham Bouchahta, et al.
Page
of 59
Search research articles
Search
Showing results (241-250 of 586) with videos related to
Sort By:
Page
of 59
Developmental Medicine and Child Neurology
|
March 16, 2007
Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3)
Sevim Balci, Aysun Unal, Ozlem Engiz, et al.
Comparative Cytogenetics
|
August 23, 2014
Genomic organization of repetitive DNAs and its implications for male karyotype and the neo-Y chromosome differentiation in Erythrinus erythrinus (Characiformes, Erythrinidae)
Cassia Fernanda Yano, Luiz Antonio Carlos Bertollo, Wagner Franco Molina, et al.
Gene
|
March 1, 2015
A cryptic three-way translocation t(10;19;11)(p12.31;q13.31;q23.3) with a derivative Y-chromosome in an infant with acute myeloblastic leukemia (M5b)
Moneeb A K Othman, Dragana Vujić, Zeljko Zecević, et al.
Journal of Genetics
|
September 21, 2023
Molecular characterization of <i>de novo</i> ring chromosome 21 in a child with seizures, growth retardation, and multiple congenital anomalies
Prafulla S Ambulkar, Thomas Liehr, Manish Jain, et al.
International Journal of Oncology
|
January 17, 2009
Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype
Madeleine Gross, Hasmik Mkrtchyan, Melanie Glaser, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2006
Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomalies
Sevim Balci, Ozlem Engiz, Dilek Aktaş, et al.
International Journal of Molecular Medicine
|
January 5, 2006
Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping and multicolor banding applying murine probes
Constanze Karst, Vladimir Trifonov, Svetlana A Romanenko, et al.
Journal of Pediatric Genetics
|
August 11, 2017
Unusual de novo Partial Trisomy 17p12p11.2 due to Unbalanced Insertion into 5p13.1 in a Severely Affected Boy
Luis Alberto Mendez-Rosado, Araceli Lantigua, Juan Galarza, et al.
Heliyon
|
December 21, 2023
CHD2 pathogenic nonsense variant in a three-generation family with variable phenotype and a paracentric inversion 16: Case report
Eleni Angelopoulou, Athina Theodosiou, Ioannis Papaevripidou, et al.
Frontiers in Genetics
|
March 11, 2024
A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature
Fatima Ouboukss, Zhour El Amrani, Hicham Bouchahta, et al.
Page
of 59