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Items: 1 to 20 of 132

1.

Inversion of chromosome 7q22 and q36 as a sole abnormality presenting in myelodysplastic syndrome: a case report.

Kaneko H, Shimura K, Kuwahara S, Ohshiro M, Tsutsumi Y, Iwai T, Horiike S, Yokota S, Ohkawara Y, Taniwaki M.

J Med Case Rep. 2014 Aug 5;8:268. doi: 10.1186/1752-1947-8-268.

2.

Translocation (2;7)(p13;q36) in a case of acute nonlymphocytic leukemia evolving from a myelodysplastic syndrome.

Sreekantaiah C, Baer MR, Solé F, Preisler HD, Sandberg AA.

Cancer Genet Cytogenet. 1988 Oct 15;35(2):199-204.

PMID:
3180021
3.

An isochromosome of the long arm of chromosome 18 in a patient with myelodysplastic syndrome with myelofibrosis.

Xue Y, Cao Y, Gao Y, Xie X, Lu D, Chen Z.

Cancer Genet Cytogenet. 1995 Feb;79(2):149-52.

PMID:
7889509
4.

Myelodysplastic syndrome preceding acute myelomonocytic leukemia with dysplastic marrow eosinophilia and inv(16).

Horiike S, Misawa S, Nishida K, Nishigaki H, Tsuda S, Taniwaki M, Takino T, Abe T.

Acta Haematol. 1989;82(3):161-4.

PMID:
2510440
5.

Spontaneous remission in myelodysplastic syndrome. A case report.

Broun ER, Heerema NA, Tricot G.

Cancer Genet Cytogenet. 1990 May;46(1):125-8.

PMID:
2331675
6.

Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias.

Fischer K, Fröhling S, Scherer SW, McAllister Brown J, Scholl C, Stilgenbauer S, Tsui LC, Lichter P, Döhner H.

Blood. 1997 Mar 15;89(6):2036-41.

7.

Acute myeloid leukemia presenting in a mother and daughter pair with the identical acquired karyotypic abnormality consisting of inversion 3q21q26 and monosomy 7: a review of possible mechanisms.

Lawrie A, Stevenson DA, Doig TN, Vickers MA, Culligan DJ.

Cancer Genet. 2012 Nov;205(11):599-602. doi: 10.1016/j.cancergen.2012.09.001. Epub 2012 Oct 12.

PMID:
23064135
8.

Three rearrangements of chromosome 5 in a patient with myelodysplastic syndrome: an atypical deletion 5q, a complex intrachromosomal rearrangement of chromosome 5, and a paracentric inversion of chromosome 5.

Douet-Guilbert N, Basinko A, Eveillard JR, Morel F, Le Bris MJ, Guéganic N, Bovo C, Herry A, Berthou C, De Braekeleer M.

Cancer Genet Cytogenet. 2010 Dec;203(2):303-8. doi: 10.1016/j.cancergencyto.2010.07.129.

PMID:
21156249
9.

Bone marrow morphology predicts additional chromosomal abnormalities in patients with myelodysplastic syndrome with del(5q).

Geyer JT, Verma S, Mathew S, Wang YL, Racchumi J, Espinal-Witter R, Subramaniyam S, Knowles DM, Orazi A.

Hum Pathol. 2013 Mar;44(3):346-56. doi: 10.1016/j.humpath.2012.05.022. Epub 2012 Sep 17.

PMID:
22995330
10.

[Chromosome 21 rearrangement in a case of therapy-related myelodysplastic syndrome in multiple myeloma].

Nakamura H, Sato T, Watanabe T, Ikeda S, Sadamori N, Ichimaru M.

Rinsho Ketsueki. 1989 Feb;30(2):216-21. Japanese.

PMID:
2746876
11.

[Myelodysplastic syndrome with multiple chromosome aberrations in a patient with Werner's syndrome].

Mita M, Ishibashi T, Shichishima T, Maruyama Y.

Rinsho Ketsueki. 1996 Aug;37(8):725-30. Review. Japanese.

PMID:
8827885
12.

Myelodysplastic syndrome with Ph negative monosomy 7 chromosome following transient bone marrow dysplasia during imatinib treatment for chronic myeloid leukemia.

Karimata K, Masuko M, Ushiki T, Kozakai T, Shibasaki Y, Yano T, Abe T, Moriyama M, Toba K, Furukawa T, Aizawa Y.

Intern Med. 2011;50(5):481-5. Epub 2011 Mar 1.

13.

[Myelodysplastic syndrome developed in a mother and her son whose bone marrow karyotype showed monosomy 7].

Wakita A, Komatsu H, Banno S, Ando M, Nitta M, Takada K, Mitomo Y, Ueda R.

Rinsho Ketsueki. 1996 Apr;37(4):311-6. Japanese.

PMID:
8847801
14.

Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasia.

Johnson EJ, Scherer SW, Osborne L, Tsui LC, Oscier D, Mould S, Cotter FE.

Blood. 1996 May 1;87(9):3579-86.

15.

Clonal karyotype evolution involving ring chromosome 1 with myelodysplastic syndrome subtype RAEB-t progressing into acute leukemia.

Duell T, Poleck-Dehlin B, Schmid C, Wunderlich B, Ledderose G, Mittermuller J, Kolb HJ, Schmetzer H.

Acta Haematol. 2006;116(2):131-6.

PMID:
16914909
16.

The unbalanced 1;7 translocation in de novo myelodysplastic syndrome and its clinical implication.

Horiike S, Taniwaki M, Misawa S, Nishigaki H, Okuda T, Yokota S, Kashima K, Inazawa J, Abe T.

Cancer. 1990 Mar 15;65(6):1350-4.

17.
18.

Structural aberrations of chromosome 7 revealed by a combination of molecular cytogenetic techniques in myeloid malignancies.

Brezinová J, Zemanová Z, Ransdorfová S, Pavlistová L, Babická L, Housková L, Melichercíková J, Sisková M, Cermák J, Michalová K.

Cancer Genet Cytogenet. 2007 Feb;173(1):10-6.

PMID:
17284364
19.

Monosomy 7 predisposes to diabetes insipidus in leukaemia and myelodysplastic syndrome.

de la Chapelle A, Lahtinen R.

Eur J Haematol. 1987 Nov;39(5):404-11. Review.

PMID:
3319680
20.

A novel recurrent chromosomal aberration involving chromosome 7 in childhood myelodysplastic syndrome.

Lizcova L, Zemanova Z, Malinova E, Jarosova M, Mejstrikova E, Smisek P, Pospisilova D, Stary J, Michalova K.

Cancer Genet Cytogenet. 2010 Aug;201(1):52-6. doi: 10.1016/j.cancergencyto.2010.05.004.

PMID:
20633770

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