Deletions of chromosome 13q in monoclonal gammopathy of undetermined significanceKÖNIGSBERG, R; ACKERMANN, J; LUDWIG, H et al.Leukemia. 2000, Vol 14, Num 11, pp 1975-1979, issn 0887-6924Article

Functional Xp disomy and de novo t(X;13) (q10;q10) in a girl with hypomelanosis of ItoCORREA-CERRO, L. S; RIVERA, H; VASQUEZ, A. I et al.Journal of medical genetics. 1997, Vol 34, Num 2, pp 161-163, issn 0022-2593Article

Fragile site and interstitial telomere repeat sequences at the fusion point of a de novo (Y;13) translocationBOUTOUIL, M; FETNI, R; QU, J et al.Human genetics. 1996, Vol 98, Num 3, pp 323-327, issn 0340-6717Article

Poor prognosis in multiple myeloma is associated only with partial or complete deletions of chromosome 13 or abnormalities involving 11q and not with other karyotype abnormalitiesTRICOT, G; BARLOGIE, B; SUNDAR JAGANNATH et al.Blood. 1995, Vol 86, Num 11, pp 4250-4256, issn 0006-4971Article

Aplastic anaemia with 13q-: a benign subset of bone marrow failure responsive to immunosuppressive therapyISHIYAMA, Ken; KARASAWA, Masamitsu; MIYAWAKI, Shuichi et al.British journal of haematology. 2002, Vol 117, Num 3, pp 747-750, issn 0007-1048Article

Chromosome 13q neocentromeres: Molecular cytogenetic characterization of three additional cases and clinical spectrumSHULAN LI; MALAFIEJ, Paul; VELAGALETI, Golpalrao V. N et al.American journal of medical genetics. 2002, Vol 110, Num 3, pp 258-267, issn 0148-7299Article

Chromosome 13 deletion in myelomaSHAUGHNESSY, J; BARLOGIE, B.Current Topics in Microbiology and Immunology. 1999, Vol 246, pp 199-203, issn 0070-217XConference Paper

Pentasomy 13q in a case of acute myelogenous leukemia (M0)RAMOND, S; CACHEUX, V; CIAUDO, M et al.Cancer genetics and cytogenetics. 1998, Vol 107, Num 1, pp 73-75, issn 0165-4608Article

Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemiaDICKER, Frank; HAFERLACH, Claudia; KERN, Wolfgang et al.Blood. 2007, Vol 110, Num 4, pp 1308-1316, issn 0006-4971, 9 p.Article

Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomaliesLORENTZ, Cindy Pham; JALAL, Syed M; THOMPSON, Dana M et al.American journal of medical genetics. 2002, Vol 111, Num 1, pp 61-67, issn 0148-7299Article

Prognostic value of cytogenetics in multiple myelomaCHUMYONG SEONG; DELASALLE, K; HAYES, K et al.British journal of haematology. 1998, Vol 101, Num 1, pp 189-194, issn 0007-1048Article

Spontaneous clinical and cytogenetic remission of aplastic anemia in a patient with del(13q)SAITOH, Takashi; SAIKI, Minoru; KUMAGAI, Takao et al.Cancer genetics and cytogenetics. 2002, Vol 136, Num 2, pp 126-128, issn 0165-4608Article

3p13 region : A possible location of a tumor suppressor gene involved in uveal melanomaBLASI, M. A; ROCCELLA, F; BALESTRAZZI, E et al.Cancer genetics and cytogenetics. 1999, Vol 108, Num 1, pp 81-83, issn 0165-4608Article

13q14 deletions are not primary events in B-cell chronic lymphocytic leukemia : A study of 100 patients using fluorescence in situ hybridizationAVET-LOISEAU, H; DEVILDER, M.-C; GARAND, R et al.Clinical cancer research. 1996, Vol 2, Num 10, pp 1673-1677, issn 1078-0432Article

A case of duplication of 13q32→qter and deletion of 18p11.32→ter with mild phenotype : Patau syndrome and duplication of 13q revisitedHELALI, N; IAFOLLA, A. K; KAHLER, S. G et al.Journal of medical genetics. 1996, Vol 33, Num 7, pp 600-602, issn 0022-2593Article

Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formationPAGE, S. L; SHIN, J.-C; HAN, J.-Y et al.Human molecular genetics (Print). 1996, Vol 5, Num 9, pp 1279-1288, issn 0964-6906Article

Molecular studies of translocations and trisomy involving chromosome 13ROBINSON, W. P; BERNASCONI, F; DUTLY, F et al.American journal of medical genetics. 1996, Vol 61, Num 2, pp 158-163, issn 0148-7299Article

Both hypodiploidy and deletion of chromosome 13 independently confer poor prognosis in multiple myelomaFASSAS, Athanasios B.-T; SPENCER, Tray; SAWYER, Jeffrey et al.British journal of haematology. 2002, Vol 118, Num 4, pp 1041-1047, issn 0007-1048Article

The prognostic significance of 13q14 deletions in chronic lymphocytic leukemiaSTAROSTIK, P; O'BRIEN, S; CHUNG, C.-Y et al.Leukemia research. 1999, Vol 23, Num 9, pp 795-801, issn 0145-2126Article

Two cases of terminal deletion of chromosome 13 : Clinical features, conventional and molecular cytogenetic analysisLUQUET, I; FAVRE, B; NADAL, N et al.Annales de génétique (Paris). 1999, Vol 42, Num 1, pp 33-39, issn 0003-3995Article

Neocentromere at 13q32 in one of two stable markers derived from a 13q21 breakRIVERA, H; VASQUEZ, A. I; GARCIA-CRUZ, D et al.American journal of medical genetics. 1999, Vol 85, Num 4, pp 385-388, issn 0148-7299Conference Paper

Trisomy 13 and myeloid malignancy - characteristic blast cell morphology : A United Kingdom Cancer Cytogenetics Group surveyMEHTA, A. B; BAIN, B. J; FITCHETT, M et al.British journal of haematology. 1998, Vol 101, Num 4, pp 749-752, issn 0007-1048Article

At least nine cases of trisomy 11q23→qter in one generation as a result of familial t(11;13) translocationSMEETS, D; VAN RAVENSWAAIJ, C; DE PATER, J et al.Journal of medical genetics. 1997, Vol 34, Num 1, pp 18-23, issn 0022-2593Article

Evidence for a familial esophageal cancer susceptibility gene on chromosome 13NAN HU; GOLDSTEIN, Alisa M; ALBERT, Paul S et al.Cancer epidemiology, biomarkers & prevention. 2003, Vol 12, Num 10, pp 1112-1115, issn 1055-9965, 4 p.Article

Detection of the PAX3-FKHR fusion gene in paediatric rhabdomyosarcoma: a reproducible predictor of outcome?ANDERSON, J; GORDON, T; MCMANUS, A et al.British journal of cancer. 2001, Vol 85, Num 6, pp 831-835, issn 0007-0920Article