Abnormalities of chromosome bands 15q13-15 in childhood acute lymphoblastic leukemiaHEEREMA, Nyla A; SATHER, Harland N; GAYNON, Paul S et al.Cancer. 2002, Vol 94, Num 4, pp 1102-1110, issn 0008-543XArticle

Complex variant 15;17 translocations in acute promyelocytic leukemia : A case report and review of three-way translocationsWAN, T. S. K; CHIM, C. S; SO, C. K et al.Cancer genetics and cytogenetics. 1999, Vol 111, Num 2, pp 139-143, issn 0165-4608Article

A de novo interstitial deletion of chromosome 15 band q25 as revealed by FISH-techniqueVERMA, R. S; KLEYMAN, S. M; GIRIDHARAN, R et al.Clinical genetics. 1996, Vol 49, Num 6, pp 303-305, issn 0009-9163Article

Extreme variant of the short arm of chormosome 15FRIEDRICH, U; CAPRANI, M; NIEBUHR, E et al.Human genetics. 1996, Vol 97, Num 6, pp 710-713, issn 0340-6717Article

Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infantMILUNSKY, J. M; WYANDT, H. E; XIN-LI HUANG et al.American journal of medical genetics. 1996, Vol 61, Num 3, pp 269-273, issn 0148-7299Article

Autistic symptoms among children and young adults with isodicentric chromosome 15RINEER, S; FINUCANE, B; SIMON, E. W et al.American journal of medical genetics. 1998, Vol 81, Num 5, pp 428-433, issn 0148-7299Article

Prenatal diagnosis of a fetus with a homologous Robertsonian translocation of chromosomes 15CHEUNG, S. W; SHAFFER, L. G; RICHARDS, C. S et al.American journal of medical genetics. 1997, Vol 72, Num 1, pp 47-50, issn 0148-7299Article

Distinct 15q genotypes in Russell-Silver and ring 15 syndromesROGAN, P. K; SEIP, J. R; DRISCOLL, D. J et al.American journal of medical genetics. 1996, Vol 62, Num 1, pp 10-15, issn 0148-7299Article

Ring chromosome 15 syndrome in an adult femaleMATSUISHI, T; YAMADA, Y; ENDO, K et al.JIDR. Journal of intellectual disability research (Print). 1996, Vol 40, Num 5, pp 478-481, issn 0964-2633Article

Additional chromosome abnormalities confer worse prognosis in acute promyelocytic leukaemiaHIORNS, L. R; SWANSBURY, G. J; MEHTA, J et al.British journal of haematology. 1997, Vol 96, Num 2, pp 314-321, issn 0007-1048Article

Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21)(q26;q22.1) by FISHNADAL, M; MORENO, S; PRITCHARD, M et al.Journal of medical genetics. 1997, Vol 34, Num 1, pp 50-54, issn 0022-2593Article

Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatmentTHOMAS, J. A; JOHNSON, J; KRAAI, T. L et al.American journal of medical genetics. 2003, Vol 119A, Num 2, pp 111-120, issn 0148-7299, 10 p.Article

Supernumerary marker chromosomes derived from chromosome 15: Analysis of 32 new casesEGGERMANN, K; MAU, U. A; BUJDOSO, G et al.Clinical genetics. 2002, Vol 62, Num 1, pp 89-93, issn 0009-9163Article

Inherited DNA amplification of the proximal 15q region : cytogenetic and molecular studiesMIGNON, C; PARENTE, F; STAVROPOULOU, C et al.Journal of medical genetics. 1997, Vol 34, Num 3, pp 217-222, issn 0022-2593Article

A boy with developmental delay and a maternally inherited delection in 15q11q13KING, M; HARDY, C; ASENBAUER, B et al.Journal of medical genetics. 1996, Vol 33, Num 5, pp 422-425, issn 0022-2593Article

Incidence and implication of additional chromosome aberrations in acute promyelocytic leukaemia with translocation t(15;17)(q22;q21) : a report on 50 patientsSCHOCH, C; HAASE, D; HAFERLACH, T et al.British journal of haematology. 1996, Vol 94, Num 3, pp 493-500, issn 0007-1048Article

Mosaic tetrasomy 15q25→qter in a newborn infant with multiple anomaliesVAN DEN ENDEN, A; VERSCHRAEGEN-SPAE, M. R; VAN ROY, N et al.American journal of medical genetics. 1996, Vol 63, Num 3, pp 482-485, issn 0148-7299Article

Effect of additional chromosomal abnormalities in acute promyelocytic leukemia treated with all-trans-retinoic acid : A report of 17 patientsOKOSHI, Yasushi; AKIYAMA, Hideki; KONO, Natsu et al.International journal of hematology. 2001, Vol 73, Num 4, pp 496-501, issn 0925-5710Article

Comparative genomic hybridization of microdissected familial ovarian carcinoma : Two deleted regions on chromosome 15q not previously identified in sporadic ovarian carcinomaZWEEMER, Ronald P; RYAN, Andy; KENEMANS, Peter et al.Laboratory investigation. 2001, Vol 81, Num 10, pp 1363-1370, issn 0023-6837Article

A new case of t(5;15)(p15;q11∼q13) in infant acute lymphoblastic leukemiaSILVA, Maria Luiza M; DANTAS DE BRITO, Gilena; SIMOES, Felippe et al.Cancer genetics and cytogenetics. 2001, Vol 130, Num 1, pp 87-88, issn 0165-4608Article

Translocation (4;15)(p16;q24) : A novel reciprocal translocation in a patient with BCR/ABL negative myeloproliferative syndrome progressing to blastic phasePAPADOPOULOS, K. P; MURTY, V. V. V; LIN, N et al.Cancer genetics and cytogenetics. 1999, Vol 111, Num 1, pp 18-20, issn 0165-4608Article

A sole del(15q) anomaly in post-myelodysplasia acute myeloid leukemiaYAHATA, N; OHYASHIKI, K; IWASE, O et al.Leukemia research. 1998, Vol 22, Num 9, pp 845-847, issn 0145-2126Article

Translocation t(15;17) in acute myelogenous leukemia with atypical megakaryoblastic features : Diagnostic, clinical, and therapeutic implicationsMORGAN, D. L; DUNN, D. M; COBOS, E et al.Cancer genetics and cytogenetics. 1996, Vol 92, Num 1, pp 50-53, issn 0165-4608Article

Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardationFLEJTER, W. L; BENNETT-BAKER, P. E; MOHAMMAD GHAZIUDDIN et al.American journal of medical genetics. 1996, Vol 61, Num 2, pp 182-187, issn 0148-7299Article

Insulin-like growth factor I receptor expression and function in fibroblasts from two patients with deletion of the distal long arm of chromosome 15SIEBLER, T; LOPACZYNSKI, W; NISSLEY, P et al.The Journal of clinical endocrinology and metabolism. 1995, Vol 80, Num 12, pp 3447-3457, issn 0021-972XArticle