467 related articles for article (PubMed ID: 16259325)
21. Partial trisomy 13 in an infant with a mild phenotype: application of fluorescence in situ hybridization in cytogenetic syndromes.
Begovic D; Hitrec V; Lasan R; Letica L; Baric I; Sarnavka V; Galic S
Croat Med J; 1998 Jun; 39(2):212-5. PubMed ID: 9575279
[TBL] [Abstract][Full Text] [Related]
22. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
[TBL] [Abstract][Full Text] [Related]
23. Distal partial trisomy 1q: report of two cases and a review of the literature.
Utine GE; Aktas D; Alanay Y; Gücer S; Tuncbilek E; Mrasek K; Liehr T
Prenat Diagn; 2007 Sep; 27(9):865-71. PubMed ID: 17605151
[TBL] [Abstract][Full Text] [Related]
24. Partial trisomy 15q: report of a patient and literature review.
Chandler K; Schrander-Stumpel CT; Engelen J; Theunissen P; Fryns JP
Genet Couns; 1997; 8(2):91-7. PubMed ID: 9219006
[TBL] [Abstract][Full Text] [Related]
25. Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection.
Delatycki MB; Voullaire L; Francis D; Petrovic V; Robertson A; Webber LM; Slater HR
J Med Genet; 1999 Apr; 36(4):335-8. PubMed ID: 10227406
[TBL] [Abstract][Full Text] [Related]
26. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM
Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721
[TBL] [Abstract][Full Text] [Related]
27. [Molecular cytogenetic detection of partial chromosome 13q trisomy and its relation with the clinical features of tortilcollis].
Du J; Tan YQ; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Jun; 20(3):189-92. PubMed ID: 12778440
[TBL] [Abstract][Full Text] [Related]
28. [Trisomy 4p as result of a maternal translocation t(4;8)(q11;p23)].
Stumm M; Reuter M; Mandon U; Brückner R; Wieacker P
Klin Padiatr; 1999; 211(1):35-9. PubMed ID: 10067217
[TBL] [Abstract][Full Text] [Related]
29. Molecular cytogenetic analysis of chromosome aberrations in desmoid tumors.
Mayer M; Kulig A; Sygut J; Dziki A; Simon D; Latos-Bieleńska A; Ferenc T
Pol J Pathol; 2007; 58(3):167-71. PubMed ID: 18074861
[TBL] [Abstract][Full Text] [Related]
30. A de novo 8q22.2-24.3 duplication in a patient with mild phenotype.
Concolino D; Iembo MA; Moricca MT; Rapsomaniki M; Marotta R; Galesi O; Fichera M; Romano C; Strisciuglio P
Eur J Med Genet; 2012 Jan; 55(1):67-70. PubMed ID: 21971480
[TBL] [Abstract][Full Text] [Related]
31. Trisomy of medial 15q as result of an analphoid supernumerary ring chromosome detected by CGH and FISH.
Constantinou M; Płowás I; Kałuzewski B
Cytogenet Genome Res; 2007; 119(1-2):165-9. PubMed ID: 18160798
[TBL] [Abstract][Full Text] [Related]
32. A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter-->22q12.1: clinical, cytogenetic and molecular observations.
Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Maher TA; Quadrelli R
Eur J Med Genet; 2008; 51(4):332-42. PubMed ID: 18316257
[TBL] [Abstract][Full Text] [Related]
33. Duplication 20p identified via fluorescent in situ hybridization.
LeChien KA; McPherson E; Estop AM
Am J Med Genet; 1994 Apr; 50(2):187-9. PubMed ID: 7516625
[TBL] [Abstract][Full Text] [Related]
34. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
[TBL] [Abstract][Full Text] [Related]
35. A familial complex chromosome translocation resulting in duplication of 6p25.
Vermeesch JR; Thoelen R; Fryns JP
Ann Genet; 2004; 47(3):275-80. PubMed ID: 15337473
[TBL] [Abstract][Full Text] [Related]
36. World Health Organization classification in combination with cytogenetic markers improves the prognostic stratification of patients with de novo primary myelodysplastic syndromes.
Bernasconi P; Klersy C; Boni M; Cavigliano PM; Calatroni S; Giardini I; Rocca B; Zappatore R; Caresana M; Dambruoso I; Lazzarino M; Bernasconi C
Br J Haematol; 2007 May; 137(3):193-205. PubMed ID: 17408458
[TBL] [Abstract][Full Text] [Related]
37. Trisomy chromosome (22)(q13.1-qter) as a result of paternal inversion (22)(p11q13.1) proved using region-specific FISH probes.
Hou JW
Chang Gung Med J; 2005 Sep; 28(9):657-61. PubMed ID: 16323558
[TBL] [Abstract][Full Text] [Related]
38. Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies.
Ergun MA; Balci S; Konaç E; Kan D; Menevşe S; Bartsch O
Turk J Pediatr; 2004; 46(4):384-7. PubMed ID: 15641279
[TBL] [Abstract][Full Text] [Related]
39. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
[TBL] [Abstract][Full Text] [Related]
40. Probing the human genome in search for a new 3q syndrome.
Azar GM; Conte RA; Kleyman SM; Logush AZ; Verma RS
Ann Genet; 1999; 42(2):95-100. PubMed ID: 10434123
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
