251 related articles for article (PubMed ID: 17567547)
61. Molecular cytogenetic characterization of a metastatic lung sarcomatoid carcinoma: 9p23 neocentromere and 9p23-p24 amplification including JAK2 and JMJD2C.
Italiano A; Attias R; Aurias A; Pérot G; Burel-Vandenbos F; Otto J; Venissac N; Pedeutour F
Cancer Genet Cytogenet; 2006 Jun; 167(2):122-30. PubMed ID: 16737911
[TBL] [Abstract][Full Text] [Related]
62. A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man.
Guanciali-Franchi P; Calabrese G; Morizio E; Gatta V; Palka C; Stuppia L; Zuffardi O
Eur J Med Genet; 2008; 51(3):239-44. PubMed ID: 18378203
[TBL] [Abstract][Full Text] [Related]
63. Parental origin of the isochromosome 12p in Pallister-Killian syndrome: molecular analysis of one patient and review of the reported cases.
Struthers JL; Cuthbert CD; Khalifa MM
Am J Med Genet; 1999 May; 84(2):111-5. PubMed ID: 10323734
[TBL] [Abstract][Full Text] [Related]
64. Multiple congenital abnormalities in a newborn with two supernumerary marker chromosomes derived from chromosome 14.
Faas BH; Van Der Deure J; Wunderink MI; Merkx G; Brunner HG
Genet Couns; 2006; 17(3):349-57. PubMed ID: 17100204
[TBL] [Abstract][Full Text] [Related]
65. Variability of origin for the neocentromeric sequences in analphoid supernumerary marker chromosomes of well-differentiated liposarcomas.
Italiano A; Maire G; Sirvent N; Nuin PA; Keslair F; Foa C; Louis C; Aurias A; Pedeutour F
Cancer Lett; 2009 Jan; 273(2):323-30. PubMed ID: 18823700
[TBL] [Abstract][Full Text] [Related]
66. Mosaic trisomy r(14) associated with epilepsy and mental retardation.
Tzoufi M; Kanioglou C; Dasoula A; Asproudis I; Tsatsoulis A; Sismani C; Patsalis PC; Georgiou I; Syrrou M
J Child Neurol; 2007 Jul; 22(7):869-73. PubMed ID: 17715281
[TBL] [Abstract][Full Text] [Related]
67. Application of FISH and Q-PCR techniques in breakpoint diagnostics in three cases of marker chromosomes derived from chromosome 15.
Helszer Z; Constantinou M; Nowacka J; Płucienniczak G; Płucienniczak A; Kałuzewski B
Med Sci Monit; 2001; 7(3):464-70. PubMed ID: 11386027
[TBL] [Abstract][Full Text] [Related]
68. An analphoid marker chromosome inv dup(15)(q26.1qter), detected during prenatal diagnosis and characterized via chromosome microdissection.
Mahjoubi F; Peters GB; Malafiej P; Shalhoub C; Turner A; Daniel A; Hill RJ
Cytogenet Genome Res; 2005; 109(4):485-90. PubMed ID: 15905642
[TBL] [Abstract][Full Text] [Related]
69. Pallister-Killian syndrome: Multiband FISH of tetrasomy 12p.
Gerdes AM; Hansen LK; Brandrup F; Soegaard K; Christoffersen A; Rasmussen K
Pediatr Dermatol; 2006; 23(4):378-81. PubMed ID: 16918638
[TBL] [Abstract][Full Text] [Related]
70. A neocentromere derived from a supernumerary marker deleted from the long arm of chromosome 6.
Qin N; Bartley J; Wang JC; Warburton PE
Cytogenet Genome Res; 2007; 119(1-2):154-7. PubMed ID: 18160796
[TBL] [Abstract][Full Text] [Related]
71. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.
Hartmann A; Hofmann UB; Hoehn H; Broecker EB; Hamm H
Pediatr Dermatol; 2004; 21(6):636-41. PubMed ID: 15575846
[TBL] [Abstract][Full Text] [Related]
72. Monosomy 8 rescue gave cells with a normal karyotype in a mildly affected man with 46,XY,r(8) mosaicism.
Gradek GA; Kvistad PH; Houge G
Eur J Med Genet; 2006; 49(4):292-7. PubMed ID: 16829350
[TBL] [Abstract][Full Text] [Related]
73. Analphoid de novo marker chromosome inv dup(3)(q28qter) with neocentromere in a dysmorphic and developmentally retarded girl.
Barbi G; Spaich C; Adolph S; Kehrer-Sawatzki H
J Med Genet; 2003 Mar; 40(3):e27. PubMed ID: 12624156
[No Abstract] [Full Text] [Related]
74. Class II neocentromeres: a putative common neocentromere site in band 4q21.2.
Warburton PC; Barwell J; Splitt M; Maxwell D; Bint S; Ogilvie CM
Eur J Hum Genet; 2003 Oct; 11(10):749-53. PubMed ID: 14512964
[TBL] [Abstract][Full Text] [Related]
75. Mosaic inv dup(8p) marker chromosome with stable neocentromere suggests neocentromerization is a post-zygotic event.
Voullaire L; Saffery R; Earle E; Irvine DV; Slater H; Dale S; du Sart D; Fleming T; Choo KH
Am J Med Genet; 2001 Jul; 102(1):86-94. PubMed ID: 11471179
[TBL] [Abstract][Full Text] [Related]
76. A fourteen years follow-up of a case of partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12: clinical, cytogenetic and molecular observations.
Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Quadrelli R
Eur J Med Genet; 2007; 50(3):224-32. PubMed ID: 17329177
[TBL] [Abstract][Full Text] [Related]
77. Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors.
Hu J; McPherson E; Surti U; Hasegawa SL; Gunawardena S; Gollin SM
Am J Med Genet; 2002 Nov; 113(1):82-8. PubMed ID: 12400070
[TBL] [Abstract][Full Text] [Related]
78. Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: unusual chromosome 9 variant.
Lukusa T; Devriendt K; Holvoet M; Fryns JP
Am J Med Genet; 2000 Mar; 91(3):192-7. PubMed ID: 10756341
[TBL] [Abstract][Full Text] [Related]
79. Severe psychomotor retardation in a boy with a small supernumerary marker chromosome 19p.
Vraneković J; Brajenović-Milić B; Modrusan-Mozetić Z; Babić I; Kapović M
Cytogenet Genome Res; 2008; 121(3-4):298-301. PubMed ID: 18758176
[TBL] [Abstract][Full Text] [Related]
80. Pericentric inversion inv(7)(p11q21.1): report on two cases and genotype-phenotype correlations.
Vorsanova SG; Iourov IY; Demidova IA; Kolotii AD; Soloviev IV; Yurov YB
Tsitol Genet; 2006; 40(3):45-8. PubMed ID: 16933852
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
