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Cytogenetics Database CytoD 1.0

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Query: 47,xy

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47,xy     Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy. J Med Genet. 1977 Apr;14(2):114-9.
47,xy     Rare translocation 47,XY,t(12;21) in Down's syndrome. Hum Hered. 1974;24(2):160-6.
47,xy     Constitutional heteromorphism of 9q13 --> q21 in a patient with chronic myelogenous leukemia. Clin Genet. 1995 Jun;47(6):321-3.
47,xy     Partial trisomies 13 and 22 due to nondisjunction of a maternal reciprocal translocation, t(13;22)(q22;q11). Hum Genet. 1978 Nov 24;45(1):89-95.
47,xy     Chronic myelogenous leukemia with a complex Ph1 translocation in an XYY male. Cancer Genet Cytogenet. 1984 Feb;11(2):215-9.
47,xy     Extraskeletal Ewing's tumor with translocation t(11;22) in a patient with Down syndrome. Cancer Genet Cytogenet. 1989 Jan;37(1):79-84.
47,xy     Is 4q13 a recurring breakpoint in solitary fibrous tumors? Cancer Genet Cytogenet. 2001 Nov;131(1):69-73.
47,xy     Chromosome abnormalities in bone marrow of Fanconi anemia patients. Cancer Genet Cytogenet. 1993 Jan;65(1):47-50.
47,xy     Second meiotic nondisjunction of the rearranged chromosome in a familial reciprocal 5/13 translocation. Am J Med Genet. 1991 Oct 1;41(1):32-4.
47,xy     Cytogenetic findings in acute megakaryoblastic leukemia (ANLL-M7). Cancer Genet Cytogenet. 1990 Aug 1;48(1):119-23.
47,xy     Prenatal diagnosis of trisomy 9. Humangenetik. 1975 Sep 23;29(3):243-50.
47,xy     Elliptocytosis in myelodysplastic syndrome associated with translocation (1;5)(p10;q10) and deletion of 20q. Cancer Genet Cytogenet. 1999 Jan 15;108(2):162-5.
47,xy     11q23 abnormalities in children with acute nonlymphocytic leukemia (M4-M5). Association with previous chemotherapy. Cancer Genet Cytogenet. 1990 Mar;45(1):1-11.
47,xy     Higher incidence of small Y chromosome in humans with trisomy 21 (Down syndrome). Pediatr Res. 1982 Sep;16(9):769-70.
47,xy     Intratumoral cytogenetic heterogeneity in a benign neoplasm. Cancer. 1991 Jun 15;67(12):3110-6.
47,xy     Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome? Am J Med Genet. 2002 Jun 1;110(1):51-6.
47,xy     Double minute chromosomes contain amplified c-myc oncogene sequences in acute myeloid leukemia. Hematopathol Mol Hematol. 1996;10(4):193-9.
47,xy     Isolation of a cosmid clone corresponding to an inv(21) breakpoint of a patient with transient abnormal myelopoiesis. Am J Hum Genet. 1996 Mar;58(3):544-50.
47,xy     American Burkitt lymphoma stage II with 47,XY,+20,t(8;14)(q24;q32). Cancer Genet Cytogenet. 1990 Sep;48(2):275-7.
47,xy     A 14-year-old girl with Turner syndrome of complicated karyotype; 45,X/47,XY,+18,-19,+der(19),t(Y;19)(q12;p13.3). Jinrui Idengaku Zasshi. 1985 Dec;30(4):307-11.
47,xy     Case of acute monocytic leukemia with 47,XY,+X,t(2;10)(q21.1;q26.1) and basophilia. Cancer Genet Cytogenet. 1996 Jan;86(1):80-2.
47,xy     Deletion of specific sequences or modification of centromeric chromatin are responsible for Y chromosome centromere inactivation. Hum Genet. 1990 Oct;85(5):491-4.
47,xy     Kleeblattsch├Ądel anomaly and partial trisomy for chromosome 13 (47,XY,+der(13),t(3,13)(q24; q14). Clin Genet. 1980 Jun;17(6):409-14.
47,xy     Sequential development of distinct clonal chromosome abnormalities in a patient with preleukaemia. Br J Haematol. 1985 Mar;59(3):411-8.
47,xy     Cytogenetic triclonality in acute myeloid leukemia: a morphologic, immunologic and in situ hybridization study. Cancer Genet Cytogenet. 1994 Feb;72(2):86-91.
47,xy     Examination of fetal cells and cell-free fetal DNA in maternal blood for fetal gender determination. Gynecol Obstet Invest. 2004;58(1):57-60. Epub 2004 May 19.
47,xy     Prenatal diagnosis of mosaic tetrasomy 21q confirmed by fluorescence in situ hybridization. Clin Genet. 1997 Apr;51(4):260-3.
47,xy     Acute monocytic leukemia with translocation t(1;11) (p31;q23): simultaneous staining of chromosomes and cell surface antigens. Haematol Blood Transfus. 1990;33:145-9.
47,xy     Change in cellular phenotype from lymphoid to erythroid in a case of ALL. Scand J Haematol. 1980 Feb;24(2):115-21.
47,xy     47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22. Hum Genet. 1977 Jun 10;37(1):111-6.
47,xy     Molecular cytogenetic characterization of two small chromosome 8 derived supernumerary mosaic markers. Am J Med Genet. 2004 Jul 1;128A(1):33-8.
47,xy     A case of partial trisomy 13 presenting with hyperinsulinaemic hypoglycaemia. Hong Kong Med J. 2003 Oct;9(5):381-3.
47,xy     Publication Types: Case Reports 1 disjunction.
47,xy     Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat. J Med Genet. 1975 Sep;12(3):305-7.
47,xy     Mosaic trisomy 19 syndrome. Ann Genet. 1981;24(1):32-3.
47,xy     Trisomy 6 in a childhood acute mixed lineage leukemia. Acta Paediatr Jpn. 1998 Dec;40(6):616-20.
47,xy     Tertiary trisomy due to a reciprocal translocation of chromosomes 5 and 21 in a four-generation family. Am J Med Genet. 2000 Jun 19;92(5):311-7.
47,xy     Supernumerary ring marker chromosome as a secondary rearrangement in a parapharyngeal lipoma with t(10;12)(q25;q15) as the primary karyotypic abnormality. Cancer Genet Cytogenet. 1992 Dec;64(2):163-5.
47,xy     Ring chromosome 22 and neurofibromatosis. Clin Genet. 1992 Oct;42(4):171-7.
47,xy     Three interesting cases of Down's syndrome. Ann Genet. 1983;26(2):123-8.
47,xy     First case of trisomy 13 plus mosaic trisomy 1q. Fetal Diagn Ther. 2002 May-Jun;17(3):133-6.
47,xy     Norplant-2 subdermal contraceptive system: experience in Taiwan. J Formos Med Assoc. 1993 May;92(5):446-50.
47,xy     Tertiary trisomy 14q--, due to paternal balanced translocation 46,XY,t(1;14)(q44;q22). Hum Genet. 1979 Jun 19;49(2):175-8.
47,xy     Pentasomy 8q resulting from duplication of isochromosome 8q in chronic myelomonocytic leukemia. Leuk Lymphoma. 2002 Jan;43(1):207-10.
47,xy     A case of lipoblastoma with t(3;8)(q12;q11.2). Cancer Genet Cytogenet. 1992 Aug;62(1):103-5.
47,xy     Pericentric inversions of chromosome number 9: benign or harmful? Hum Hered. 1979;29(2):111-7.
47,xy     Down-Turner syndrome: case report and review. J Med Genet. 1994 Oct;31(10):807-10.
47,xy     Unfavourable outcome of a patient with M2 acute non lymphocytic leukemia and a 47,XY,t(5;7)(q34;q21), +8 karyotype. Haematologica. 1991 Jan-Feb;76(1):65-8.
47,xy     Myelodysplastic syndrome with trisomy 8 in an adolescent with Fanconi anaemia and selective IgA deficiency. Am J Hematol. 1989 Aug;31(4):280-3.
47,xy     Characterisation of a collecting duct carcinoma by cytogenetic analysis and comparative genomic hybridisation. Int J Oncol. 1998 Sep;13(3):461-4.
47,xy     Holoprosencephaly and trisomy 13 in a fetus with maternal early gestational amphetamine abuse--a case report. Gaoxiong Yi Xue Ke Xue Za Zhi. 1993 Dec;9(12):703-6.
47,xy     The establishment of a cell line (NH-AR) from a human nodular lymphoma and a comparison with lymphoblastoid cell line. Cancer. 1980 Dec 1;46(11):2438-45.
47,xy     Demonstration of acquired hemizygosity and clonality in acute lymphoblastic leukemia with chromosome 7 abnormalities using hypervariable DNA probes. Genes Chromosomes Cancer. 1990 Jul;2(2):88-93.
47,xy     Trisomy 8 syndrome. A psychological and somatic study of a mentally non-retarded male with 46,XY/47,XY,+8 chromosome constitution. Clin Genet. 1977 Oct;12(4):227-32.
47,xy     Maternal translocation t(13:18)(q34:q11) and Edward's syndrome in a fetus: 47,xy,t(13:18)(q34:q11) + 18. Clin Genet. 1984 Nov;26(5):481-4.
47,xy     Abnormal chromosome 9 in a neonate program. Report of three cases. Arch Pathol Lab Med. 1990 Feb;114(2):185-7.
47,xy     Fluorescence in situ hybridization reveals trisomy 2q by insertion into 9p in hepatoblastoma. Cancer Genet Cytogenet. 1998 Apr 15;102(2):148-50.
47,xy     Comment in: Hum Genet. 1992 Sep-Oct;90(1-2):191-2. Hum Genet. 1992 Feb;88(4):482-3.
47,xy     46,XY del(18)(q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q- syndrome. Clin Genet. 1993 Feb;43(2):76-8.
47,xy     Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization. Am J Med Genet. 1995 Mar 27;56(2):219-33.
47,xy     Lockwood DH, Farrier A, Hecht F, Allanson J. 1 segregation in first meiosis.
47,xy     Cytogenetic heterogeneity in a clear cell hidradenoma of the skin. Cancer Genet Cytogenet. 1994 Oct;77(1):26-32.
47,xy     Comment in: Am J Med Genet. 2000 Jul 17;93(2):166-8. Am J Med Genet. 1992 Oct 1;44(3):288-92.
47,xy     Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2. Hum Genet. 1991 Sep;87(5):561-6.
47,xy     An unusual cytogenetic abnormality involving chromosomes 1 and 7 in a case of chronic myelomonocytic leukemia. Cancer Genet Cytogenet. 1995 Nov;85(1):75-7.
47,xy     [Non-immunologic hydrops fetalis (NIHF)--case report of double partial trisomy 15q and 17q resulting from familial translocation 15/17 and cytogenetic findings in 50 cases with hydrops fetalis] Klin Padiatr. 1987 Jul-Aug;199(4):309-14.
47,xy     Trisomy 4 leading to duplication of a mutated KIT allele in acute myeloid leukemia with mast cell involvement. Cancer Genet Cytogenet. 2000 May;119(1):26-31.
47,xy     Cryptic insertion of MLL gene into 9p22 leads to MLL-MLLT3 (AF9) fusion in a case of acute myelogenous leukemia. Genes Chromosomes Cancer. 2004 Aug;40(4):349-54.
47,xy     A recurrent nonrandom translocation (3;7)(q27;p12) associated with BCL-6 gene rearrangement in B-cell diffuse large cell lymphoma. Cancer Genet Cytogenet. 1998 Jul 1;104(1):19-27.
47,xy     Inflammatory myofibroblastic tumor of bone: report of two cases with evidence of clonal chromosomal changes. Am J Surg Pathol. 1997 Oct;21(10):1166-72.
47,xy     A low rate of trisomy 21 in twin-pregnancies: a cytogenetics retrospective study of 278 cases. Genet Couns. 2003;14(4):395-400.
47,xy     Myelodysplastic syndrome transforming to acute promyelocytic-like leukemia with trisomy and rearrangement of chromosome 11. Genes Chromosomes Cancer. 1994 May;10(1):15-25.
47,xy     Prenatal diagnosis of partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21) (p13.3;q21). Prenat Diagn. 1997 Jul;17(7):675-80.
47,xy     Fetal blood chromosome analysis: some new indications for prenatal karyotyping. Br J Obstet Gynaecol. 1985 Sep;92(9):915-20.
47,xy     Mosaic supernumerary inv dup(15) chromosome with four copies of the P gene in a boy with pigmentary dysplasia. Am J Med Genet. 2004 Apr 30;126A(3):290-2.
47,xy     AML with unusual chromosomal changes. Translocation (15;21) and 5q- in the presence of two normal chromosomes 5. Cancer Genet Cytogenet. 1992 Jul 15;61(2):139-41.
47,xy     Acute promyelocytic leukemia in Crohn's disease. Case report and review of the literature. J Clin Gastroenterol. 1991 Jun;13(3):325-7.
47,xy     Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype. Prenat Diagn. 2003 Feb;23(2):128-33.
47,xy     Clonal rearrangement of 15p11.2, 16p11.2, and 16p13.3 in a case of nodular fasciitis: additional evidence favoring nodular fasciitis as a benign neoplasm and not a reactive tumefaction. Cancer Genet Cytogenet. 2002 Dec;139(2):138-40.
47,xy     A lineage-specific t(1;14)(q21;q32) as an early event in development of B-cell clonal expansion. Cancer Genet Cytogenet. 1992 Dec;64(2):166-9.
47,xy     Comment in: Intern Med. 1998 Mar;37(3):235. Intern Med. 1998 Mar;37(3):320-3.
47,xy     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.
47,xy     der(1)t(1;19)(p12;p11): a new nonrandom chromosomal abnormality in myelodysplastic syndrome. Cancer Genet Cytogenet. 1997 Apr;94(2):85-7.
47,xy     Significance of abnormalities of chromosomes 5 and 8 in chondroblastoma. Clin Orthop. 1998 Apr;(349):189-93.
47,xy     Congenital Diaphragmatic Hernia and Chromosomal Anomalies: Autopsy Study. Pediatr Dev Pathol. 2004 Mar 4; [Epub ahead of print]
47,xy     Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13-cen. Am J Med Genet. 1996 Oct 2;65(1):56-9.
47,xy     Identification of novel chromosomal rearrangements in acute myelogenous leukemia involving loci on chromosome 2p23, 15q22 and 17q21. Leukemia. 1999 Oct;13(10):1534-8.
47,xy     Cytogenetic evidence for extramedullary blast crisis with t(8;13)(q11;p11) in chronic myelomonocytic leukemia. Acta Haematol. 1992;88(4):201-3.
47,xy     Class II neocentromeres: a putative common neocentromere site in band 4q21.2. Eur J Hum Genet. 2003 Oct;11(10):749-53.
47,xy     Myelodysplastic syndrome with clonal eosinophilia accompanied by eosinophilic pulmonary interstitial infiltration. Acta Haematol. 2000;104(2-3):119-23.
47,xy     Acute promyelocytic leukemia with additional chromosomal abnormalities and absence of Auer rods. Am J Clin Pathol. 1999 Jul;112(1):113-8.
47,xy     Leukemia in a trisomy 21 mosaic: specific involvement of the trisomic cells. Cancer Genet Cytogenet. 1986 Feb 1;20(1-2):109-13.
47,xy     A human T cell line with an abnormal trisomy 2 karyotype established by coculture of peripheral lymphocytes with an HTLV-II-infected simian leukocyte cell line. Acta Pathol Jpn. 1993 May;43(5):237-43.


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