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Cytogenetics Database CytoD 1.0

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Query: del(9)(p?)

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del(9)(q     Involvement of the long arm of chromosome 9 in medulloblastoma in an adult. Cancer Genet Cytogenet. 1997 Jul 1;96(1):81-4.
del(9p),     Jumping translocation of chromosome 14 in a skin squamous cell carcinoma from a xeroderma pigmentosum patient. Cancer Genet Cytogenet. 1988 Jul 1;33(1):29-33.
del(9p).     Choanal atresia in a patient with the deletion (9p) syndrome. Am J Med Genet. 1994 Jan 1;49(1):88-90.
del(9)(q     Schizophrenia and mental retardation in an adult male with a de novo interstitial deletion 9(q32q34.1). J Med Genet. 1991 Apr;28(4):282-3.
del(9)(p2     Karyotypic evolution: cytogenetics follow-up study in childhood acute lymphoblastic leukemia. Asian Pac J Cancer Prev. 2003 Aug-Dec;4(4):358-68.
del(9p)      Parental origin of De Novo chromosome 9 deletions in del(9p) syndrome. Am J Med Genet. 1995 May 22;57(1):79-81.
del(9)(p2     Chromosome abnormalities in low-grade central nervous system tumors. Cancer Genet Cytogenet. 1992 May;60(1):67-73.
del(9)(p1     Revision of the chromosome anomalies of the T-cell malignant cell line peer. Ann Genet. 1990;33(2):76-8.
del(9).      Acute nonlymphocytic leukemia following lung cancer in a patient with a constitutional supernumerary chromosome. Cancer Genet Cytogenet. 1988 Oct 15;35(2):263-8.
del(9)(q     Cytogenetic findings in acute megakaryoblastic leukemia (ANLL-M7). Cancer Genet Cytogenet. 1990 Aug 1;48(1):119-23.
del(9)(p2     Acquired chromosome rearrangements, including fine interstitial deletions, in a patient with Down syndrome and monoblastic leukemia. Pediatrics. 1984 Dec;74(6):1029-33.
del(9)(q     Leukemic transformation with trisomy 8 in essential thrombocythemia: a report of four cases. Eur J Haematol. 2002 Feb;68(2):112-6.
del(9) (     [Acute myelomonocytic leukemia (M4) with CD19 antigen expression, eosinophilia and basophilia in bone marrow] Rinsho Ketsueki. 1989 May;30(5):726-30.
del(9)(q     Cytogenetic biclonality corresponding to multiphasic differentiation in an atypical thyroid adenoma. Cancer Genet Cytogenet. 1994 Nov;78(1):102-4.
del(9)(p1     Deletion (9) (p13.1 p21.1). Am J Med Genet. 2000 Mar 13;91(2):113-5.
del(9)(q     9p monosomy in a patient with Gilles de la Tourette's syndrome. Neurology. 1991 Sep;41(9):1513-5.
del(9)(p1     Novel chromosome findings in bladder cancer cell lines detected with multiplex fluorescence in situ hybridization. Cancer Genet Cytogenet. 2002 Jun;135(2):139-46.
del(9)(pt     Newborn infant with del(9)(pter----q32:) and multiple congenital anomalies including arrhinencephaly, cardiac malformations, and rudimentary ears. Am J Med Genet Suppl. 1987;3:161-6.
del(9)(p1     Clonal chromosome aberrations in three sacral chordomas. Cancer Genet Cytogenet. 1994 Apr;73(2):147-51.
del(9q),     Comment in: Blood. 2000 Sep 1;96(5):2002. Blood. 1998 Oct 1;92(7):2322-33.
del(9)(p2     Abnormalities of the short arm of chromosome 9 with partial loss of material in hematological disorders. Leukemia. 1987 Jul;1(7):541-8.
del(9)(p2     Specific minor chromosome deletions in myelodysplastic syndromes: clinical and morphologic correlations. Cancer Genet Cytogenet. 1987 Jun;26(2):227-34.
del(9p),     Analysis of chromosome aberrations in cell lines derived from laryngeal cancer in relation to tumor progression. Eur Arch Otorhinolaryngol. 2002 May;259(5):269-73. Epub 2002 Apr 24.
del(9)(q     Novel clonal der(8)t(8;14)(p11;q11),del(9)(q13q22) and t(14;22) (q13;q13) in a patient with fulminant adult T-cell leukemia/lymphoma. Cancer Genet Cytogenet. 2002 Nov;139(1):34-7.
del(9p).     Brief clinical report: two children with de novo del(9p). Am J Med Genet. 1983 Apr;14(4):751-7.
del(9).      Translocation (8;21) and its variants in acute nonlymphocytic leukemia. The relative importance of chromosomes 8 and 21 to the genesis of the disease. Cancer Genet Cytogenet. 1988 Jul 15;33(2):161-73.
del(9p).     Molecular and cytogenetic characterization of 9p- abnormalities. Am J Med Genet. 1993 May 15;46(3):288-92.
del(9)(q     A case of transitional cell carcinoma of the bladder with a del(9)(q11q21.2). Cancer Genet Cytogenet. 1993 Aug;69(1):76-7.
del(9)(9     Interstitial deletion of chromosome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome. Eur J Pediatr. 2003 Feb;162(2):100-3. Epub 2002 Dec 10.
del(9p),     Cytogenetic biclonality in malignant hematologic disorders. Cancer Genet Cytogenet. 1992 Aug;62(1):25-8.
del(9p)      A mild phenotype associated with der(9)t(3;9) (p25;p23). J Med Genet. 1996 Jul;33(7):625-7.
del(9q)      6p+ and 9q- in two chromosomally distinct clones occurring in a case of myelodysplastic syndrome evolving to acute nonlymphocytic leukemia. Cancer Genet Cytogenet. 1988 Oct 15;35(2):213-21.
del(9)(pt     De novo interstitial deletion in the long arm of chromosome 9: a new chromosome syndrome. J Med Genet. 1982 Feb;19(1):68-70.
del(9p)      Comment in: Am J Med Genet. 1992 Sep 15;44(2):244-5. Am J Med Genet. 1988 Jan;29(1):43-8.
del(9p)      The INSL4 gene maps close to WI-5527 at 9p24.1-->p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome. Cytogenet Cell Genet. 1998;81(3-4):275-7.
del(9)(q     Malignant solitary fibrous tumor of the pleura: report of a case with cytogenetic analysis. Virchows Arch. 2003 Apr;442(4):388-92. Epub 2003 Feb 27.
del(9)(q     Karyotypic findings in two cases of male breast cancer. Cancer Genet Cytogenet. 2000 Sep;121(2):190-3.
del(9)(q     Terminal deletion of the long arm of chromosome 9 in acute promyelocytic leukemia with a cryptic PML/RAR alpha rearrangement. Cancer Genet Cytogenet. 1999 Sep;113(2):120-5.
del(9q),     Influence of cytogenetic abnormalities on outcome after allogeneic bone marrow transplantation for acute myeloid leukemia in first complete remission. Biol Blood Marrow Transplant. 2002;8(8):435-43.
del(9)(q     UM-EC-1, a new hypodiploid human cell line derived from a poorly differentiated endometrial cancer. Cancer Res. 1988 Apr 1;48(7):1864-73.
del(9)(q     Interstitial 9q deletion in T-lymphoid/myeloid biphenotypic leukaemia. Br J Haematol. 1992 Feb;80(2):172-7.
del(9p),     Abnormalities of chromosome bands 13q12 to 13q14 in childhood acute lymphoblastic leukemia. J Clin Oncol. 2000 Nov 15;18(22):3837-44.
del(9q)      A study to determine whether trisomy 8, deleted 9q and trisomy 22 are markers of cryptic rearrangements of PML/RARalpha, AML1/ETO and CBFB/MYH11 respectively in acute myeloid leukaemia. MRC Adult Leukaemia Working Party. Medical Research Council. Br J Haematol. 1998 May;101(2):338-40.
del(9)(q     Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32). J Med Genet. 1994 Feb;31(2):156-8.
del(9)(q     An interstitial deletion of chromosome 9 in a girl with multiple congenital anomalies. J Med Genet. 1977 Dec;14(6):455-9.
del(9p)      9p deletion and distal 9q duplication due to a paternal pericentric inversion 9(p22q32). Jinrui Idengaku Zasshi. 1991 Mar;36(1):111-6.
del(9)(p2     Gonadoblastoma in a patient with del(9)(p22) and sex reversal: report of a case and review of the literature. Cancer Genet Cytogenet. 2003 Jun;143(2):174-7.
del(9q)      Cytogenetic investigation of transitional cell carcinomas of the upper urinary tract. Cancer Genet Cytogenet. 1999 Oct 15;114(2):117-20.
del(9q)(     Classical and molecular cytogenetic abnormalities and outcome of childhood acute myeloid leukaemia: report from a referral centre in Israel. Br J Haematol. 2004 Aug;126(3):320-37.
del(9q)      Concomitant presence of trisomy 21 and del(9q) in acute myeloid leukemia. Cancer Genet Cytogenet. 1992 Nov;64(1):92-4.
del(9p)      NOR activity and centromere suppression related in a de novo fusion tdic(9;13)(p22;p13) chromosome in a child with del(9p) syndrome. Am J Med Genet. 1985 Nov;22(3):577-84.
del(9p)      Eleven new cases of del(9p) and features from 80 cases. J Med Genet. 1988 Nov;25(11):741-9.
del(9) (     Comment in: Am J Med Genet. 2001 Apr 15;100(1):84. Am J Med Genet. 2000 Aug 14;93(4):305-12.
del(9q)      Fifty-one patients with acute myeloid leukemia and translocation t(8;21)(q22;q22): an additional deletion in 9q is an adverse prognostic factor. Leukemia. 1996 Aug;10(8):1288-95.
del(9p)      Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias. Eur J Haematol. 2000 Jul;65(1):40-51.
del(9)(q     Establishment of a leukaemic cell line from a patient with acquisition of chromosomal abnormalities during disease progression in myelodysplastic syndrome. Br J Haematol. 1993 Nov;85(3):469-76.
del(9)/-     Unrelated clonal chromosome abnormalities in myelodysplastic syndromes and acute myeloid leukemias. Cancer Genet Cytogenet. 2002 Jan 15;132(2):156-8.
del(9)(p1     [Analysis of the factors associated with prognosis in patients with Ph chromosome positive adult acute lymphoblastic leukemia] Zhonghua Xue Ye Xue Za Zhi. 2004 Jul;25(7):417-20.
del(9)(q     Chromosomal abnormalities in non-neoplastic renal tissue. Cancer Genet Cytogenet. 1995 Dec;85(2):152-4.
del(9)(p1     Nonrandom chromosomal aberrations and cytogenetic heterogeneity in gallbladder carcinomas. Genes Chromosomes Cancer. 1999 Dec;26(4):312-21.
del(9)(q     A case of acute megakaryocytic leukemia presenting as peripheral acute leukemia with complex karyotypic abnormalities. Cancer Genet Cytogenet. 1998 Aug;105(1):83-5.
del(9)(p2     Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines. Cytogenet Genome Res. 2002;98(2-3):118-25.
del(9q)      Apparently unrelated clones shown by spectral karyotyping to represent clonal evolution of cryptic t(10;11)(p13;q23) in a patient with acute monoblastic leukemia. Cancer Genet Cytogenet. 2000 Jul 15;120(2):105-10.
del(9),      Genome-wide analysis of sixteen chordomas by comparative genomic hybridization and cytogenetics of the first human chordoma cell line, U-CH1. Genes Chromosomes Cancer. 2001 Nov;32(3):203-11.
del(9)(q     Cytogenetic analysis of a primary salivary gland myoepithelioma. Cancer Genet Cytogenet. 1999 Aug;113(1):49-53.
del(9)(q     Consistent interstitial chromosomal deletions in myeloid malignancies and their correlation with fragile sites. Cancer Genet Cytogenet. 1993 Jan;65(1):51-7.
del(9p)      Dup(4p)del(9p) in a familial mental retardation syndrome. Resemblance to de Lange syndrome detected by high-resolution banding. Am J Dis Child. 1985 Jan;139(1):81-4.
del(9)(q     Cytogenetic, cytomorphologic, and immunologic analysis in 55 children with acute lymphoblastic leukemia. Cancer Genet Cytogenet. 1996 May;88(1):57-65.
del(9)(q     Two cases of acute myeloblastic leukemia (M2 type) with karyotypes 45X,-X,t(6;8)(q27;q22),inv(9) and 46,XY,t(8;21)(q22;q22),del(9)(q22). Cancer Genet Cytogenet. 1985 Oct;18(2):105-11.
del(9)(p2     Ossifying fibromyxoid tumor of soft parts. Cytogenetic findings. Cancer Genet Cytogenet. 2002 Mar;133(2):124-8.
del(9q),     Secondary chromosomal abnormalities in acute leukemias. Leukemia. 1994 Jun;8(6):953-62.
del(9p)      A cluster of familial malignant mesothelioma with del(9p) as the sole chromosomal anomaly. Cancer Genet Cytogenet. 2002 Oct 1;138(1):73-6.
del(9) (     Detection of minimal residual disease in an AML patient with trisomy 8 using interphase fish. Pathology. 1997 Aug;29(3):289-93.
del(9)(p2     Paternal isodisomy 7q secondary to monosomy 7 at recurrence in a Down syndrome child with acute myelogenous leukemia. Cancer Genet Cytogenet. 2002 Apr 15;134(2):138-41.
del(9p),     Frequency and clinical significance of cytogenetic abnormalities in pediatric T-lineage acute lymphoblastic leukemia: a report from the Children's Cancer Group. J Clin Oncol. 1998 Apr;16(4):1270-8.
del(9q)      Secondary chromosome aberrations in the acute leukemias. Cancer Genet Cytogenet. 1986 Aug;22(4):331-8.
del(9q),     Cytogenetic correlation with disease status and treatment outcome in advanced stage leukemia post bone marrow transplantation: a Southwest Oncology Group study (SWOG-8612). Leuk Res. 1995 Jun;19(6):381-8.
del(9)(p1     Relationship between chromosomal changes complexity and disease aggressiveness in myeloid and lymphoid disorders. J Cell Mol Med. 2002 Jul-Sep;6(3):389-98.
del(9)(p2     Chromosomal changes and correspondingly altered proto-oncogene expression in human gliomas. Value of combined cytogenetic and molecular genetic analysis. Anticancer Res. 1993 Jan-Feb;13(1):113-8.
del(9)(q     A case of M2 acute myeloblastic leukemia associated with an interstitial 9q deletion. Cancer Genet Cytogenet. 1987 Jan;24(1):177-80.
del(9)(q     Interstitial 9q deletion is associated with CD7+ acute leukemia of myeloid and T lymphoid lineage. Leukemia. 1996 Dec;10(12):1990-2.
del(9)(q     Two cases of AML (M2) with a t(8;19)(q22;q13): a new cytogenetic variant. Cancer Genet Cytogenet. 2000 Apr 15;118(2):154-8.
del(9p)      Cytogenetic analysis in mantle cell lymphoma: a review of 214 cases. Leuk Lymphoma. 2002 Apr;43(4):783-91.
del(9)(q     Establishment of an undifferentiated leukemia cell line (Kasumi-3) with t(3;7)(q27;q22) and activation of the EVI1 gene. Jpn J Cancer Res. 1996 Mar;87(3):269-74.

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