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A new mosaic der(18)t(1;18)(q32.1;q21.3) with developmental delay and facial dysmorphism
Young-Jin Choi, Eunsim Shin, Tae Sik Jo, Jin-Hwa Moon, Se-Min Lee, Joo-Hwa Kim, Jae-Won Oh, Chang-Ryul Kim, In Joon Seol
Clin Exp Pediatr. 2016;59(2):91-95.   Published online February 29, 2016

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A new mosaic der(18)t(1;18)(q32.1;q21.3) with developmental delay and facial dysmorphism
Korean Journal of Pediatrics. 2016;59(2):91   Crossref logo

Combined immunodeficiency, facial dysmorphism, optic nerve atrophy, skeletal anomalies and developmental delay: a new syndrome
Clinical Genetics. 2009;76(5):449-457   Crossref logo
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Derivative (3)t(3;18)(q27;q21)t(18;16)(q21;?) involving the BCL2 and BCL6 genes in follicular lymphoma with t(3;14;18)(q27;q32;q21)
Cancer Genetics and Cytogenetics. 2007;179(1):69-75   Crossref logo
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More evidence on TRIO missense mutations in the spectrin repeat domain causing severe developmental delay and recognizable facial dysmorphism with macrocephaly
neurogenetics. 2021;22(3):221-224   Crossref logo
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Follicular lymphoma with trisomy 18 and over-expression of BCL2 in the absence of t(14;18)(q32;q21)
Cancer Genetics and Cytogenetics. 2000;123(1):52-54   Crossref logo
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Acute leukemia with t(1;3)(p36;q21), evolution to t(1;3)(p36;q21),t(14;17)(q32;q21), and loss of red cell A and Leb antigens
Cancer Genetics and Cytogenetics. 1992;64(1):80-85   Crossref logo
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Triple-hit B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma associated with a novel complex karyotype including t(2;3)(q21;q27), t(8;14)(q24;q32) and t(14;18)(q32;q21)
British Journal of Haematology. 2012;160(5):569-569   Crossref logo
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Secondary cytogenetic abnormalities associated with a t(14:18)(q32;q21) in non-Hodgkin's lymphomas
Cancer Genetics and Cytogenetics. 1991;56(1):116   Crossref logo
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Acquisition of a t(11;14)(q13;q32) in clonal evolution in a follicular lymphoma with a t(14;18)(q32;q21) and t(3;22)(q27;q11.2)
Cancer Genetics. 2015;208(6):303-309   Crossref logo
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A translocation 46,XY,t(1;2)(q32;q21) in a male with reproductive failure
Human Genetics. 1985;70(1):93-93   Crossref logo
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