138 related articles for article (PubMed ID: 11169558)
21. Wilms tumor, AML and medulloblastoma in a child with cancer prone syndrome of total premature chromatid separation and Fanconi anemia.
Sari N; Akyuz C; Aktas D; Gumruk F; Orhan D; Alikasifoglu M; Aydin B; Alanay Y; Buyukpamukcu M
Pediatr Blood Cancer; 2009 Aug; 53(2):208-10. PubMed ID: 19373780
[TBL] [Abstract][Full Text] [Related]
22. [Centromere separation and malignancy].
Méhes K
Orv Hetil; 2000 Nov; 141(46):2479-81. PubMed ID: 11126679
[TBL] [Abstract][Full Text] [Related]
23. High risk of malignancy in mosaic variegated aneuploidy syndrome.
Hunter A
Am J Med Genet A; 2003 Mar; 117A(2):199. PubMed ID: 12567425
[No Abstract] [Full Text] [Related]
24. A case report of a fetus with mosaic autosomal variegated aneuploidies and literature review.
Cho CH; Oh MJ; Lim CS; Lee CK; Cho Y; Yoon SY
Ann Clin Lab Sci; 2015; 45(1):106-9. PubMed ID: 25696020
[TBL] [Abstract][Full Text] [Related]
25. Mosaic variegated aneuploidy with microcephaly: a new human mitotic mutant?
Warburton D; Anyane-Yeboa K; Taterka P; Yu CY; Olsen D
Ann Genet; 1991; 34(3-4):287-92. PubMed ID: 1809239
[TBL] [Abstract][Full Text] [Related]
26. Premature separation of centromere and aneuploidy: an indicator of high risk in unaffected individuals from familial breast cancer families?
Rao NM; Joshi NN; Shinde SR; Advani SH; Ghosh SN
Eur J Cancer Prev; 1996 Oct; 5(5):343-50. PubMed ID: 8972253
[TBL] [Abstract][Full Text] [Related]
27. Studies of mitotic and centromeric abnormalities in Roberts syndrome: implications for a defect in the mitotic mechanism.
Jabs EW; Tuck-Muller CM; Cusano R; Rattner JB
Chromosoma; 1991 May; 100(4):251-61. PubMed ID: 2055135
[TBL] [Abstract][Full Text] [Related]
28. Recapitulation of the Roberts syndrome cellular phenotype by inhibition of INCENP, ZWINT-1 and ZW10 genes.
Musio A; Mariani T; Montagna C; Zambroni D; Ascoli C; Ried T; Vezzoni P
Gene; 2004 Apr; 331():33-40. PubMed ID: 15094189
[TBL] [Abstract][Full Text] [Related]
29. Ring chromosome 6: case report and review of literature.
Kini KR; Van Dyke DL; Weiss L; Logan MS
Hum Genet; 1979; 50(2):145-9. PubMed ID: 511129
[TBL] [Abstract][Full Text] [Related]
30. Tetrasomy 21pter-->q21.2 in a male infant without typical Down's syndrome dysmorphic features but moderate mental retardation.
Rost I; Fiegler H; Fauth C; Carr P; Bettecken T; Kraus J; Meyer C; Enders A; Wirtz A; Meitinger T; Carter NP; Speicher MR
J Med Genet; 2004 Mar; 41(3):e26. PubMed ID: 14985397
[No Abstract] [Full Text] [Related]
31. Variegated aneuploidy in two siblings: phenotype, genotype, CENP-E analysis, and literature review.
Flejter WL; Issa B; Sullivan BA; Carey JC; Brothman AR
Am J Med Genet; 1998 Jan; 75(1):45-51. PubMed ID: 9450856
[TBL] [Abstract][Full Text] [Related]
32. Syndrome of microcephaly, deafness/malformed ears, mental retardation and peculiar facies in a mother and son.
Kawashima H; Tsuji N
Clin Genet; 1987 May; 31(5):303-7. PubMed ID: 3608216
[TBL] [Abstract][Full Text] [Related]
33. Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?
Tolmie JL; Boyd E; Batstone P; Ferguson-Smith ME; al Roomi L; Connor JM
Hum Genet; 1988 Oct; 80(2):197-200. PubMed ID: 3169747
[TBL] [Abstract][Full Text] [Related]
34. Partial trisomy 12q24.31----qter.
Tajara EH; Varella-Garcia M; Gusson AC
J Med Genet; 1985 Feb; 22(1):73-6. PubMed ID: 3981585
[TBL] [Abstract][Full Text] [Related]
35. Total aneuploidy and age-related sex chromosome aneuploidy in cultured lymphocytes of normal men and women.
Fitzgerald PH; McEwan CM
Hum Genet; 1977 Dec; 39(3):329-37. PubMed ID: 598841
[TBL] [Abstract][Full Text] [Related]
36. [Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].
Bocian E; Nowakowska B; Obersztyn E; Borg K; Chudoba I; Kostyk E; Kruczek A; Pietrzyk J; Mazurczak T
Med Wieku Rozwoj; 2006; 10(1 Pt 2):211-25. PubMed ID: 17028390
[TBL] [Abstract][Full Text] [Related]
37. The phenotype of ring chromosome 3.
Wilson GN; Pooley J; Parker J
J Med Genet; 1982 Dec; 19(6):471-3. PubMed ID: 7154048
[TBL] [Abstract][Full Text] [Related]
38. Ring chromosome 13 syndrome.
Fried K; Rosenblatt M; Mundel G; Krikler R
Clin Genet; 1975 Mar; 7(3):203-8. PubMed ID: 1139790
[TBL] [Abstract][Full Text] [Related]
39. Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.
Miller JQ
Neurology; 1973 Nov; 23(11):1141-6. PubMed ID: 4795737
[No Abstract] [Full Text] [Related]
40. Tetrasomy 21pter-q22.11: molecular, cytogenetic, and clinical findings.
Cerretini R; Luccerini V; Stivel M; Bañares V; Aranda I; Alba L; Pivetta O; Slavutsky I
Clin Genet; 1999 Apr; 55(4):283-6. PubMed ID: 10361993
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
