Results 121 to 130 of about 91,924 (199)

Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentromeric heterochromatin of chromosomes 13, 21 and 18 [PDF]

, 1986
Bakker, E., Cornelisse, J. L., Cremer, Thomas, Devilee, P., Hager, H. D., Pearson, P., Scholl, Hans Peter, Slagboom, P., Stevenson, A. F. G.   +8 more
core  

Recent advances in the detection technologies for balanced chromosomal rearrangements. [PDF]

Front Genet
Gao M, Ren J, Liu S.
europepmc   +1 more source

Recurrent Chromosome Destabilization Through Repeat-Mediated Rearrangements in a Fungal Pathogen. [PDF]

Genome Biol Evol
Fouché S, Oggenfuss U, McDonald BA, Croll D.   +3 more
europepmc   +1 more source

Prenatal diagnosis of a complex chromosomal rearrangement involving five chromosomes

Clinical and Experimental Obstetrics & Gynecology, 2018
Hongjun Li, Qi Zhao, Jian Ke, Zuliang Shi, Dan Lu, Bo Wang   +5 more
openaire   +1 more source

Spectrum and Clinical Reproductive Significance of Cytogenetic Abnormalities in Infertility and Recurrent Early Pregnancy Loss: A Five-Year Retrospective Study of 10,285 Cases. [PDF]

Cureus
Kunda S, Kasaragadda M, Patibandla S, Singh S, Parvez S, Rao Golla T.   +5 more
europepmc   +1 more source

Chromoanagenesis and cancer: mechanisms and consequences of localized, complex chromosomal rearrangements. [PDF]

Nat Med, 2012
Holland AJ, Cleveland DW.
europepmc   +1 more source

Elucidating the pathogenic mechanism of a pedigree with complex rearrangements on chromosome 4 using optical genome mapping technology: a study on the genetics and functional pathways in a child with developmental delay. [PDF]

Mol Cytogenet
Qin J, Zeng Y, Qin S, Wang W, Huang J, Wei X, Chang R, Zheng X, Li Y, Yuan D, Wei X.   +10 more
europepmc   +1 more source

Cytogenetics in the genomics era: why karyotyping still matters. [PDF]

BMC Med Genomics
Chebly A.
europepmc   +1 more source

Optical Genome Mapping Enhances Structural Variant Detection and Refines Risk Stratification in Chronic Lymphocytic Leukemia. [PDF]

Genes (Basel)
Chakraborty SR, Bickford MA, Smuliac NA, Tonseth KA, Bao J, Murad F, Domínguez Vigil IG, Steinmetz HB, Wainman LM, Shah P, Bengtson EM, PonnamReddy S, Harmon GA, Donnelly LL, Tafe LJ, Karrs JX, Kaur P, Khan WA.   +17 more
europepmc   +1 more source

Intrachromosomal insertion as a diagnostic challenge: a hidden structural rearrangement causing recurrent duplication and deletion. [PDF]

Mol Cytogenet
Kawamura R, Shichiri Y, Suzuki H, Murase Y, Naru Y, Hara T, Tsuboi A, Satano H, Sugihara E, Kurahashi H.   +9 more
europepmc   +1 more source