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Items: 1 to 20 of 25

1.

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
2.

Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival.

Bödör C, Renneville A, Smith M, Charazac A, Iqbal S, Etancelin P, Cavenagh J, Barnett MJ, Kramarzová K, Krishnan B, Matolcsy A, Preudhomme C, Fitzgibbon J, Owen C.

Haematologica. 2012 Jun;97(6):890-4. doi: 10.3324/haematol.2011.054361. Epub 2012 Jan 22.

3.

Familial myelodysplastic syndromes: a review of the literature.

Liew E, Owen C.

Haematologica. 2011 Oct;96(10):1536-42. doi: 10.3324/haematol.2011.043422. Epub 2011 May 23. Review.

4.

Familial childhood monosomy 7 and associated myelodysplasia.

Gaitonde S, Boumendjel R, Angeles R, Rondelli D.

J Pediatr Hematol Oncol. 2010 Aug;32(6):e236-7. doi: 10.1097/MPH.0b013e3181e75759.

PMID:
20661156
5.

Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome.

Jongmans MC, Kuiper RP, Carmichael CL, Wilkins EJ, Dors N, Carmagnac A, Schouten-van Meeteren AY, Li X, Stankovic M, Kamping E, Bengtsson H, Schoenmakers EF, van Kessel AG, Hoogerbrugge PM, Hahn CN, Brons PP, Scott HS, Hoogerbrugge N.

Leukemia. 2010 Jan;24(1):242-6. doi: 10.1038/leu.2009.210. Epub 2009 Oct 15. No abstract available.

PMID:
19946261
6.

Identification of a common microdeletion cluster in 7q21.3 subband among patients with myeloid leukemia and myelodysplastic syndrome.

Asou H, Matsui H, Ozaki Y, Nagamachi A, Nakamura M, Aki D, Inaba T.

Biochem Biophys Res Commun. 2009 May 29;383(2):245-51. doi: 10.1016/j.bbrc.2009.04.004. Epub 2009 Apr 7.

PMID:
19358830
7.

Somatic CEBPA mutations are a frequent second event in families with germline CEBPA mutations and familial acute myeloid leukemia.

Pabst T, Eyholzer M, Haefliger S, Schardt J, Mueller BU.

J Clin Oncol. 2008 Nov 1;26(31):5088-93. doi: 10.1200/JCO.2008.16.5563. Epub 2008 Sep 2.

PMID:
18768433
8.

Familial myelodysplasia and acute myeloid leukaemia--a review.

Owen C, Barnett M, Fitzgibbon J.

Br J Haematol. 2008 Jan;140(2):123-32. doi: 10.1111/j.1365-2141.2007.06909.x. Review.

PMID:
18173751
9.

Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR.

Porta G, Maserati E, Mattarucchi E, Minelli A, Pressato B, Valli R, Zecca M, Bernardo ME, Lo Curto F, Locatelli F, Danesino C, Pasquali F.

Leukemia. 2007 Aug;21(8):1833-5. Epub 2007 Apr 26. No abstract available.

PMID:
17460707
10.

Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia: an international retrospective study.

Hasle H, Alonzo TA, Auvrignon A, Behar C, Chang M, Creutzig U, Fischer A, Forestier E, Fynn A, Haas OA, Harbott J, Harrison CJ, Heerema NA, van den Heuvel-Eibrink MM, Kaspers GJ, Locatelli F, Noellke P, Polychronopoulou S, Ravindranath Y, Razzouk B, Reinhardt D, Savva NN, Stark B, Suciu S, Tsukimoto I, Webb DK, Wojcik D, Woods WG, Zimmermann M, Niemeyer CM, Raimondi SC.

Blood. 2007 Jun 1;109(11):4641-7. Epub 2007 Feb 13.

11.

HIC gene, a candidate suppressor gene within a minimal region of loss at 7q31.1 in myeloid neoplasms.

Cigognini D, Corneo G, Fermo E, Zanella A, Tripputi P.

Leuk Res. 2007 Apr;31(4):477-82. Epub 2006 Oct 24.

PMID:
17064770
12.

The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease.

Kratz CP, Niemeyer CM, Castleberry RP, Cetin M, Bergsträsser E, Emanuel PD, Hasle H, Kardos G, Klein C, Kojima S, Stary J, Trebo M, Zecca M, Gelb BD, Tartaglia M, Loh ML.

Blood. 2005 Sep 15;106(6):2183-5. Epub 2005 May 31.

13.

Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22.

Curtiss NP, Bonifas JM, Lauchle JO, Balkman JD, Kratz CP, Emerling BM, Green ED, Le Beau MM, Shannon KM.

Genomics. 2005 May;85(5):600-7.

PMID:
15820312
14.

Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies.

Minelli A, Maserati E, Rossi G, Bernardo ME, De Stefano P, Cecchini MP, Valli R, Albano V, Pierani P, Leszl A, Sainati L, Lo Curto F, Danesino C, Locatelli F, Pasquali F.

Genes Chromosomes Cancer. 2004 Jul;40(3):165-71.

PMID:
15138996
15.

Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects.

Maserati E, Minelli A, Menna G, Cecchini MP, Bernardo ME, Rossi G, De Filippi P, Lo Curto F, Danesino C, Locatelli F, Pasquali F.

Cancer Genet Cytogenet. 2004 Jan 15;148(2):155-8.

PMID:
14734230
16.

Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator gene.

Minelli A, Maserati E, Giudici G, Tosi S, Olivieri C, Bonvini L, De Filippi P, Biondi A, Lo Curto F, Pasquali F, Danesino C.

Cancer Genet Cytogenet. 2001 Jan 15;124(2):147-51.

PMID:
11172908
17.

Myelodysplastic syndrome associated with monosomy 7 in a child with Bloom syndrome.

Aktas D, Koc A, Boduroglu K, Hicsonmez G, Tuncbilek E.

Cancer Genet Cytogenet. 2000 Jan 1;116(1):44-6.

PMID:
10616531
18.

Juvenile myelomonocytic leukemia and Noonan syndrome.

Choong K, Freedman MH, Chitayat D, Kelly EN, Taylor G, Zipursky A.

J Pediatr Hematol Oncol. 1999 Nov-Dec;21(6):523-7. Review.

PMID:
10598665
19.
20.

Monosomy 7 myelodysplastic syndrome and other second malignant neoplasms in children with neurofibromatosis type 1.

Maris JM, Wiersma SR, Mahgoub N, Thompson P, Geyer RJ, Hurwitz CG, Lange BJ, Shannon KM.

Cancer. 1997 Apr 1;79(7):1438-46.

PMID:
9083167

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