140 related articles for article (PubMed ID: 31411529)
1. Acquired centromeric heteromorphism of chromosome 7 yields discordant results between fluorescent in situ hybridization and karyotype analysis in a child with severe congenital neutropenia.
Farra C; Raimondi S; Abboud M
Pediatr Hematol Oncol; 2019 Oct; 36(7):432-437. PubMed ID: 31411529
[TBL] [Abstract][Full Text] [Related]
2. Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemia.
Sokolic RA; Ferguson W; Mark HF
Cancer Genet Cytogenet; 1999 Dec; 115(2):106-13. PubMed ID: 10598142
[TBL] [Abstract][Full Text] [Related]
3. Spurious monosomy 7 in leukemia due to centromeric heteromorphism.
Duval A; Feneux D; Sutton L; Tchernia G; Léonard C
Cancer Genet Cytogenet; 2000 May; 119(1):67-9. PubMed ID: 10812174
[TBL] [Abstract][Full Text] [Related]
4. Acquired X-chromosome aneuploidy in children with acute lymphoblastic leukemia.
Heinonen K; Mahlamäki E; Riikonen P; Meltoranta RL; Rahiala J; Perkkiö M
Med Pediatr Oncol; 1999 May; 32(5):360-5. PubMed ID: 10219338
[TBL] [Abstract][Full Text] [Related]
5. A Next-Generation Sequencing Test for Severe Congenital Neutropenia: Utility in a Broader Clinicopathologic Spectrum of Disease.
McNulty SN; Evenson MJ; Riley M; Yoest JM; Corliss MM; Heusel JW; Duncavage EJ; Pfeifer JD
J Mol Diagn; 2021 Feb; 23(2):200-211. PubMed ID: 33217554
[TBL] [Abstract][Full Text] [Related]
6. Fluorescence in situ hybridisation studies to characterise complete and partial monosomy 7 in myeloid disorders.
Gibbons B; Lillington DM; Monard S; Young BD; Cheung KL; Lister TA; Kearney L
Genes Chromosomes Cancer; 1994 Aug; 10(4):244-9. PubMed ID: 7522537
[TBL] [Abstract][Full Text] [Related]
7. Genomic instability in bone marrow failure syndromes.
Kearns WG; Sutton JF; Maciejewski JP; Young NS; Liu JM
Am J Hematol; 2004 Jul; 76(3):220-4. PubMed ID: 15224355
[TBL] [Abstract][Full Text] [Related]
8. Centromeric fragment of chromosome 7 in atypical chronic myeloid leukemia with the SET binding protein 1 gene mutation.
Coccaro N; Tota G; Anelli L; Zagaria A; Casieri P; Cellamare A; Minervini A; Minervini CF; Brunetti C; Ricco A; Orsini P; Cumbo C; Specchia G; Albano F
Leuk Lymphoma; 2015 Mar; 56(3):826-8. PubMed ID: 24991718
[No Abstract] [Full Text] [Related]
9. Analysis of chromosome aneuploidy in breast carcinoma progression by using fluorescence in situ hybridization.
Mendelin J; Grayson M; Wallis T; Visscher DW
Lab Invest; 1999 Apr; 79(4):387-93. PubMed ID: 10211991
[TBL] [Abstract][Full Text] [Related]
10. Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics.
Beyer V; Castagné C; Mühlematter D; Parlier V; Gmür J; Hess U; Kovacsovics T; Meyer-Monard S; Tichelli A; Tobler A; Jacky E; Schanz U; Bargetzi M; Hagemeijer A; de Witte T; van Melle G; Jotterand M
Cancer Genet Cytogenet; 2004 Jul; 152(1):29-41. PubMed ID: 15193439
[TBL] [Abstract][Full Text] [Related]
11. Class II Analphoid Chromosome in a Child with Aberrant Chromosome 7: A Rare Cytogenetic Association.
Kumar MJ; Kumar RA; Subhashree V; Jayasudha T; Hemagowri V; Koshy T; Gowrishankar K
Cytogenet Genome Res; 2015; 146(2):120-123. PubMed ID: 26226839
[TBL] [Abstract][Full Text] [Related]
12. Aneuploidy in human sperm: results of two-and three-color fluorescence in situ hybridization using centromeric probes for chromosomes 1, 12, 15, 18, X, and Y.
Spriggs EL; Rademaker AW; Martin RH
Cytogenet Cell Genet; 1995; 71(1):47-53. PubMed ID: 7606926
[TBL] [Abstract][Full Text] [Related]
13. Severe congenital neutropenia with elastase, neutrophil expressed (ELANE) gene mutation in a Tanzanian child.
Shoo A; Swai P; Kindole C; Ngailo E; Godfrey E; Massawe E; Warren AJ; Luzzatto L
Br J Haematol; 2022 Mar; 196(5):1271-1274. PubMed ID: 34725814
[No Abstract] [Full Text] [Related]
14. Chromosomal aberrations in congenital bone marrow failure disorders--an early indicator for leukemogenesis?
Göhring G; Karow A; Steinemann D; Wilkens L; Lichter P; Zeidler C; Niemeyer C; Welte K; Schlegelberger B
Ann Hematol; 2007 Oct; 86(10):733-9. PubMed ID: 17653548
[TBL] [Abstract][Full Text] [Related]
15. Estimation of aneuploidy for chromosomes 3, 7, 16, X and Y in spermatozoa from 10 normospermic men using fluorescence in-situ hybridization.
Downie SE; Flaherty SP; Swann NJ; Matthews CD
Mol Hum Reprod; 1997 Sep; 3(9):815-9. PubMed ID: 9358009
[TBL] [Abstract][Full Text] [Related]
16. Detection of monosomy 7 in bone marrow by fluorescence in situ hybridization. A study of Fanconi anemia patients and review of the literature.
Thurston VC; Ceperich TM; Vance GH; Heerema NA
Cancer Genet Cytogenet; 1999 Mar; 109(2):154-60. PubMed ID: 10087952
[TBL] [Abstract][Full Text] [Related]
17. Fluorescence in situ hybridization analysis of minute marker chromosomes in leukemia with monosomy 7.
Viguié F; Prigent Y; Ramond S; Baumelou E; Cadiou M; Dreyfus F; Zittoun R
Leukemia; 1995 Jul; 9(7):1154-8. PubMed ID: 7630189
[TBL] [Abstract][Full Text] [Related]
18. Confirmation of centromeric fusion in 7p/1q translocation associated with myelodysplastic syndrome.
Hoo JJ; Szego K; Jones B
Cancer Genet Cytogenet; 1992 Dec; 64(2):186-8. PubMed ID: 1486571
[TBL] [Abstract][Full Text] [Related]
19. An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.
Iourov IY; Soloviev IV; Vorsanova SG; Monakhov VV; Yurov YB
J Histochem Cytochem; 2005 Mar; 53(3):401-8. PubMed ID: 15750029
[TBL] [Abstract][Full Text] [Related]
20. Role of multicolor fluorescence in situ hybridization (FISH) in simultaneous detection of probe sets for chromosome 18, X and Y in uncultured amniotic fluid cells.
Kim JI; Rhee JH
J Korean Med Sci; 1999 Aug; 14(4):438-42. PubMed ID: 10485625
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
