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Interstitial deletion 2P accompanied by marker chromosome formation of the deleted segment resulting in a stable acentric marker chromosomePETIT, P; FRYNS, J. P.Genetic counseling. 1997, Vol 8, Num 4, pp 341-343, issn 1015-8146Conference Paper

Mental retardation with rare fragile site expressed at 2q11TÜKÜN, Ajlan; RENDA, Yavuz; TOPCU, Meral et al.Brain & development (Tokyo. 1979). 2000, Vol 22, Num 8, pp 498-500, issn 0387-7604Article

Structural abnormalities of chromosome 2 in benign thyroid tumors : Three new cases and review of the literatureBOL, S; BELGE, G; THODE, B et al.Cancer genetics and cytogenetics. 1999, Vol 114, Num 1, pp 75-77, issn 0165-4608Article

Genetic linkage of Welander distal myopathy to chromosome 2p13AHLBERG, G; VON TELL, D; BORG, K et al.Annals of neurology. 1999, Vol 46, Num 3, pp 399-404, issn 0364-5134Conference Paper

Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2SAAL, H. M; KING, L. J; ZIMMERMAN, D et al.American journal of medical genetics. 1996, Vol 66, Num 4, pp 373-377, issn 0148-7299Article

Interstitial duplication of the short arm of chromosome 2 : report of a new case and reviewMEGARBANE, A; SOURATY, N; PRIEUR, M et al.Journal of medical genetics. 1997, Vol 34, Num 9, pp 783-786, issn 0022-2593Article

A specific chromosome aberration in a keratoacanthomaKIM, Dae-Kwang; KIM, Joo-Young; KIM, Hyeung-Tae et al.Cancer genetics and cytogenetics. 2003, Vol 142, Num 1, pp 70-72, issn 0165-4608, 3 p.Article

Chromosome 2q duplications : Case report of a de novo interstitial duplication and review of the literatureBIRD, Lynne M; MASCARELLO, James T.American journal of medical genetics. 2001, Vol 100, Num 1, pp 13-24, issn 0148-7299Article

Trisomy 2q11.2→q21,1 resulting from an unbalanced insertion in two generationsGLASS, I. A; STORMER, P; OEI, P. T. S. P et al.Journal of medical genetics. 1998, Vol 35, Num 4, pp 319-322, issn 0022-2593Article

Interstitial deletion 2(p11.2p13) : a rare chromosomal abnormalityWENGER, S. L; MCPHERSON, E. W.Clinical genetics. 1997, Vol 52, Num 1, pp 61-62, issn 0009-9163Article

Two sibs with partial trisomy 2qBARNICOAT, A. J; ABUSAAD, I; MACKIE, C. M et al.American journal of medical genetics. 1997, Vol 70, Num 2, pp 166-170, issn 0148-7299Article

Biphenotypic leukemia with a new translocation, t(2;6)(q31;q23)TAGUCHI, H; MORISHITA, N; MURAKAMI, k et al.Cancer genetics and cytogenetics. 1996, Vol 91, Num 2, pp 104-105, issn 0165-4608Conference Paper

Circulating t(2;5)-positive cells can be detected in cord blood of healthy newbornsLAURENT, C; LOPEZ, C; DESJOBERT, C et al.Leukemia. 2012, Vol 26, Num 1, pp 188-190, issn 0887-6924, 3 p.Article

Gingival fibromatosis and partial duplication of the short arm of chromosome 2 dup(2)(p13→p21)FRYNS, J. P.Annales de génétique (Paris). 1996, Vol 39, Num 1, pp 54-55, issn 0003-3995Article

Deletion or triplication of the α3 (VI) collagen gene in three patients with 2q37 chromosome aberrations and symptoms of collagen-related disordersRAUCH, A; PFEIFFER, R. A; TRAUTMANN, U et al.Clinical genetics. 1996, Vol 49, Num 6, pp 279-285, issn 0009-9163Article

Allelic loss on chromosomes 2q21 and 19p13.2 in oxyphilic thyroid tumorsSTANKOV, Karmen; PASTORE, Alessandro; PAPOTTI, Mauro et al.International journal of cancer. 2004, Vol 111, Num 3, pp 463-467, issn 0020-7136, 5 p.Article

Preimplantation genetic diagnosis for a known cryptic translocation: Follow-up clinical report and implication of segregation productsMCKENZIE, L. J; CISNEROS, P. L; TORSKY, S et al.American journal of medical genetics. 2003, Vol 121A, Num 1, pp 56-59, issn 0148-7299, 4 p.Article

Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: A cause of minute terminal chromosomal imbalancesDANIEL, Art; BAKER, Elizabeth; CHIA, Nicole et al.American journal of medical genetics. 2003, Vol 117A, Num 1, pp 57-64, issn 0148-7299, 8 p.Article

Investigation of linkage on chromosome 2q and hand and knee osteoarthritisGILLASPY, Emma; SPRECKLEY, Kristian; WALLIS, Gillian et al.Arthritis and rheumatism. 2002, Vol 46, Num 12, pp 3386-3387, issn 0004-3591, 2 p.Article

Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q)ALBRECHT, Beate; MERGENTHALER, Susanne; EGGERMANN, Katja et al.Journal of medical genetics. 2001, Vol 38, Num 3, pp 214-215, issn 0022-2593Article

Case of partial duplication 2q3 with characteristic phenotype : Rare occurrence of an unbalanced offspring resulting from a parental pericentric inversionANGLE, B; HERSH, J. H; YEN, F et al.American journal of medical genetics. 2000, Vol 91, Num 2, pp 126-130, issn 0148-7299Article

The mobile nature of acrocentric elements illustrated by three unusual chromosome variantsREDDY, K. S; SULCOVA, V.Human genetics. 1998, Vol 102, Num 6, pp 653-662, issn 0340-6717Article

The pathogenesis of large cell transformation in cutaneous T-cell lymphoma is not associated with t(2;5)(p23;q35) chromosomal translocationLI, G; SALHANY, K. E; ROOK, A. H et al.Journal of cutaneous pathology. 1997, Vol 24, Num 7, pp 403-408, issn 0303-6987Article

Serine phosphorylation of NPM―ALK, which is dependent on the auto-activation of the kinase activation loop, contributes to its oncogenic potentialPENG WANG; FANG WU; JINGDONG ZHANG et al.Carcinogenesis (New York. Print). 2011, Vol 32, Num 2, pp 146-153, issn 0143-3334, 8 p.Article