Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)GREENBERG, F; LEWIS, R. A; MCCLUGGAGE, C et al.American journal of medical genetics. 1996, Vol 62, Num 3, pp 247-254, issn 0148-7299Conference Paper

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

Partial trisomy 17p detected by spectral karyotypingMORELLI, S. H; DEUBLER, D. A; BROTHMAN, L. J et al.Clinical genetics. 1999, Vol 55, Num 5, pp 372-375, issn 0009-9163Article

Another case of t(17;22)(q22;q13) in an infantile dermatofibrosarcoma protuberansPEDEUTOUR, F; LACOUR, J. P; PERRIN, C et al.Cancer genetics and cytogenetics. 1996, Vol 89, Num 2, pp 175-176, issn 0165-4608Article

Significance of cytogenetic clonal evolution in chronic myelogenous leukemiaMAJLIS, A; SMITH, T. L; TALPAZ, M et al.Journal of clinical oncology. 1996, Vol 14, Num 1, pp 196-203, issn 0732-183XArticle

Characterization of a supernumerary marker derived from chromosome 17 by microdissection in an adult with MR/MCAKOZMA, C; BLANCATO, J; MECK, J et al.American journal of medical genetics. 1998, Vol 77, Num 1, pp 19-22, issn 0148-7299Article

del(17)(q25) In a patient with hairy cell leukemia : A new clonal chromosome abnormalitySUCAK, G. T; OGUR, G; TOPAL, G et al.Cancer genetics and cytogenetics. 1998, Vol 100, Num 2, pp 152-154, issn 0165-4608Article

Novel case of del(17)(q23.1q23.3) further highlights a recognizable phenotype involving deletions of chromosome (17)(q21q24)MICKELSON, E. C. R; ROBINSON, W. P; HRYNCHAK, M. A et al.American journal of medical genetics. 1997, Vol 71, Num 3, pp 275-279, issn 0148-7299Article

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

Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: Implications for carriers of paracentric inversionsYANG, S. P; BIDICHANDANI, S. I; FIJUERA, L. E et al.American journal of human genetics. 1997, Vol 60, Num 5, pp 1184-1193, issn 0002-9297Article

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

Prognostic significance of chromosome 17p deletions in childhood primitive neuroectodermal tumors (medulloblastomas) of the central nervous systemBIEGEL, J. A; JANSS, A. J; RAFFEL, C et al.Clinical cancer research. 1997, Vol 3, Num 3, pp 473-478, issn 1078-0432Article

Clonal Genetic alterations in the lungs of current and former smokersMAO, L; JIN SOO LEE; KEMP, B. L et al.Journal of the National Cancer Institute. 1997, Vol 89, Num 12, pp 857-862, issn 0027-8874Article

Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error : Case report and review of the literature on partial trisomy 17qterSARRI, C; GYFTODIMOU, J; BRØNDUM-NIELSEN, K et al.American journal of medical genetics. 1997, Vol 70, Num 1, pp 87-94, issn 0148-7299Article

Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patientsJUYAL, R. C; FIGUERA, L. E; HAUGE, X et al.American journal of human genetics. 1996, Vol 58, Num 5, pp 998-1007, issn 0002-9297Article

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

A new morphologic classification system for acute promyelocytic leukemia distinguishes cases with underlying PLZF/RARA gene rearrangementsSAINTY, D; LISO, V; MAHON, F.-X et al.Blood. 2000, Vol 96, Num 4, pp 1287-1296, issn 0006-4971Article

Molecular detection of microsatellite instability in basal cell carcinomaSARDI, J; PIAZZINI, M; PALLESCHI, G et al.Oncology reports. 2000, Vol 7, Num 5, pp 1119-1122, issn 1021-335XArticle

Translocation (12;17)(q13;q23) in de novo acute myeloid leukemia with trilineage myelodysplasiaWONG, K. F; SO, C. C; YU, P. H et al.Cancer genetics and cytogenetics. 1999, Vol 114, Num 2, pp 159-161, issn 0165-4608Article

Autosomal XX sex reversal caused by duplication of SOX9BING HUANG; SHENGBIAO WANG; YI NING et al.American journal of medical genetics. 1999, Vol 87, Num 4, pp 349-353, issn 0148-7299Article

Identification of a commonly deleted region at 17p13.3 in leukemia and lymphoma associated with 17p abnormalitySANKAR, M; TANAKA, K; KUMARAVEL, T. S et al.Leukemia. 1998, Vol 12, Num 4, pp 510-516, issn 0887-6924Article

Prenatal diagnosis of a trisomy 17p derived from a de novo non-mosaic satellited markerKULHARYA, A. S; GARCIA-HERAS, J; RADTKE, H. B et al.Clinical genetics. 1998, Vol 54, Num 5, pp 421-425, issn 0009-9163Article

Mutation, ageing, and ovarian cancerPIERETTI, M; TURKER, M. S.Lancet (British edition). 1997, Vol 349, Num 9053, pp 700-701, issn 0140-6736Article

Interphase cytogenetic demonstration of chromosome 9 loss in thick melanomasWOLFE, K. Q; SOUTHERN, S. A; HERRINGTON, C. S et al.Journal of cutaneous pathology. 1997, Vol 24, Num 7, pp 398-402, issn 0303-6987Article

Mosaic partial trisomy 17 due to a ring chromosome identified by fluorescence in situ hybridisationMORRISON, P. J; SMITH, N. M; MARTIN, K. E et al.American journal of medical genetics. 1997, Vol 68, Num 1, pp 50-53, issn 0148-7299Article