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6;9 Translocation in myelodysplastic syndromeSHAPIRA, M. Y; HIRSHBERG, B; AMIR, G et al.Cancer genetics and cytogenetics. 1999, Vol 112, Num 1, pp 57-59, issn 0165-4608Conference Paper

Constitutional mosaicism for a chromosome 9 inversion resulting in recombinant aneusomy in an offspringSHAVIRA, S. K; ORR-URTREGER, A; GAGOS, S et al.American journal of medical genetics. 1997, Vol 69, Num 4, pp 360-364, issn 0148-7299Article

Paracentric inversion of chromosome 9 with schizoaffective disorderINAYAMA, Y; YONEDA, H; FUKUSHIMA, K et al.Clinical genetics. 1997, Vol 51, Num 1, pp 69-70, issn 0009-9163Article

Variants of chromosome 9 with additional euchromatic bands : Two case reportsREDDY, K. S.American journal of medical genetics. 1996, Vol 64, Num 4, pp 536-538, issn 0148-7299Conference Paper

Acute myeloid leukaemia with cup-like nuclei associated with t(9;22)(q34;q11.2)SAKAI, Hirotaka; SATO, Kazuyuki; TSURUOKA, Yuka et al.British journal of haematology. 2013, Vol 162, Num 2, issn 0007-1048, p. 145Article

Molecular pathogenesis of Philadelphia chromosome negative myeloproliferative disordersKRALOVICS, Robert; SKODA, Radek C.Blood reviews. 2005, Vol 19, Num 1, pp 1-13, issn 0268-960X, 13 p.Article

Association of chromosome Arm 9p abnormalities with adverse risk in childhood acute lymphoblastic leukemia : A report from the Children's Cancer GroupHEEREMA, N. A; SATHER, H. N; ARTHUR, D. C et al.Blood. 1999, Vol 94, Num 5, pp 1537-1544, issn 0006-4971Article

New case of mosaic tetrasomy 9p with additional neurometabolic findingsEGGERMANN, T; ROSSIER, E; THEURER-MAINKA, U et al.American journal of medical genetics. 1998, Vol 75, Num 5, pp 530-533, issn 0148-7299Article

Chromosome segregation in a man heterozygous for a pericentric inversion, inv(9)(p11q13), analyzed by using sperm karyotyping and two-color fluorescence in situ hybridization on sperm nucleiCOLLS, P; BLANCO, J; MARTINEZ-PASARELL, O et al.Human genetics. 1997, Vol 99, Num 6, pp 761-765, issn 0340-6717Article

Heterogeneous prognostic impact of derivative chromosome 9 deletions in chronic myelogenous leukemiaKREIL, Sebastian; PFIRRMANN, Markus; HAFERLACH, Claudia et al.Blood. 2007, Vol 110, Num 4, pp 1283-1290, issn 0006-4971, 8 p.Article

Impaired male sex development in an infant with molecularly defined partial 9p monosomy : implication for a testis forming gene(s) on 9pOGATA, T; MUROYA, K; MATSUO, N et al.Journal of medical genetics. 1997, Vol 34, Num 4, pp 331-334, issn 0022-2593Article

Homozygosity for pericentric inversions of chromosome 9 : Prenatal diagnosis of two casesCOTTER, P. D; BABU, A; MCCURDY, L. D et al.Annales de génétique (Paris). 1997, Vol 40, Num 4, pp 222-226, issn 0003-3995Conference Paper

Duplication of chromosome 9 carrying a BCR/ABL chimeric gene in Philadelphia chromosome negative chronic myeloid leukemiaTAKAHASHI, N; MIURA, I; OHSHIMA, A et al.Cancer genetics and cytogenetics. 1996, Vol 89, Num 2, pp 166-169, issn 0165-4608Article

Detection of microsatellite alterations in the spectrum of melanocytic nevi in patients with or without individual or family history of melanomaBIRINDELLI, S; TRAGNI, G; BARTOLI, C et al.International journal of cancer. 2000, Vol 86, Num 2, pp 255-261, issn 0020-7136Article

Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p)PETIT, P; DEVRIENDT, K; VERMEESCH, J. R et al.Genetic counseling. 1998, Vol 9, Num 3, pp 215-221, issn 1015-8146Conference Paper

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

Moving towards a syndrome : a review of 20 cases and a new case of non-mosaic tetrasomy 9p with long-term survivalTONK, V. S.Clinical genetics. 1997, Vol 52, Num 1, pp 23-29, issn 0009-9163Article

Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24)HADDAD, B. R; LIN, A. E; WYANDT, H et al.Journal of medical genetics. 1996, Vol 33, Num 12, pp 1045-1047, issn 0022-2593Article

The breakpoints of a constitutional inversion of chromosome 9 associated with haemophagocytic lymphohistiocytosis are not linked to the disease geneARICO, M; DELLAVECCHIA, C; PIANTANIDA, M et al.British journal of haematology. 1999, Vol 104, Num 1, pp 108-110, issn 0007-1048Article

A report of a rare chromosome 9 variant with an unusual G-banding pattern in the 9qh regionTONK, V; KRISHNA, J.Indian journal of pediatrics. 1997, Vol 64, Num 1, pp 111-113, issn 0019-5456Article

A report of a child with a deletion (9)(q34.3) : a recognisable phenotype?AYYASH, H; MUELLER, R; MALTBY, E et al.Journal of medical genetics. 1997, Vol 34, Num 7, pp 610-612, issn 0022-2593Article

Characterization of a de novo t(Y;9) (q11.2;q22) by fish techniqueCONTE, R. A; KLEYMAN, S. M; KLEIN, V et al.Annales de génétique (Paris). 1996, Vol 39, Num 1, pp 10-15, issn 0003-3995Article

Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patientsSHIMKETS, R; GAILANI, M. R; SIU, V. M et al.American journal of human genetics. 1996, Vol 59, Num 2, pp 417-422, issn 0002-9297Article

Revaluation twenty-three years later of a supernumerary derivative chromosome 9YARDIN, Catherine; ESCLAIRE, Francoise; TERRO, Faraj et al.American journal of medical genetics. 2002, Vol 111, Num 2, pp 213-214, issn 0148-7299Article