These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 3621643)

  • 61. Partial trisomy for the short arm of chromosome 2 due to familial balance translocation.
    Sekhon GS; Taysi K; Rath R
    Hum Genet; 1978 Oct; 44(1):99-103. PubMed ID: 711241
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Trisomy 4p and deletion 4p- in a family having translocation, t(4p-; 12p+).
    Mortimer JG; Chewings W; Miethke P; Smith GF
    Hum Hered; 1978; 28(2):132-40. PubMed ID: 621087
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
    Gentile M; Buonadonna AL; Cariola F; Fiorente P; Valenzano MC; Guanti G
    J Med Genet; 1999 Jan; 36(1):77-82. PubMed ID: 9950374
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Pure trisomy 2p syndrome in two siblings with an unbalanced translocation and minimal terminal 12q monosomy characterized by high-density microarray.
    Martínez-Juárez A; Uribe-Figueroa L; Quintana-Palma M; Razo-Aguilera G; Sevilla-Montoya R
    Cytogenet Genome Res; 2014; 142(4):249-54. PubMed ID: 24751616
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Tetrasomy for the short arm of chromosome 12 with accessory isochromosome (+i(12p)) and a marked LDH-B gene dosage effect.
    Steinbach P; Rehder H
    Clin Genet; 1987 Jul; 32(1):1-4. PubMed ID: 3476222
    [TBL] [Abstract][Full Text] [Related]  

  • 66. A de novo reciprocal t(2;18) translocation with regular trisomy 21.
    Cyrus C; Kaur H; Koshy T; Thankanadar J; Nallathambi C
    Genet Test; 2007; 11(4):459-62. PubMed ID: 18294065
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Trisomy 9q3 syndrome: a case report and review of the literature.
    Naritomi K; Izumikawa Y; Goya Y; Gushiken M; Shiroma N; Hirayama K
    Clin Genet; 1989 Apr; 35(4):293-8. PubMed ID: 2653675
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Dicentric chromosome 13 and centromere inactivation.
    Schwartz S; Palmer CG; Weaver DD; Priest J
    Hum Genet; 1983; 63(4):332-7. PubMed ID: 6862437
    [TBL] [Abstract][Full Text] [Related]  

  • 69. 'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations.
    Brimblecombe FS; Lewis FJ; Vowles M
    J Med Genet; 1977 Aug; 14(4):271-4. PubMed ID: 926139
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature.
    Eggermann T; Schubert R; Engels H; Apacik C; Stengel-Rutkowski S; Haefliger C; Emiliani V; Ricagni C; Schwanitz G
    Ann Genet; 1999; 42(2):75-80. PubMed ID: 10434120
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family.
    de Pina Neto JM; Ferrari I
    Am J Med Genet; 1980; 5(1):25-33. PubMed ID: 7395898
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
    Rao VV; Carpenter NJ; Gucsavas M; Coldwell J; Say B
    Am J Med Genet; 1995 Jul; 58(1):50-3. PubMed ID: 7573156
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Pure trisomy 10p involving an isochromosome 10p.
    Berend SA; Shaffer LG; Bejjani BA
    Clin Genet; 1999 May; 55(5):367-71. PubMed ID: 10422809
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Complex translocation among chromosomes 2, 3, 9, 15, 18, 20 in a patient with 3p-syndrome.
    Omrani MD; Saleh Gargari S; Azizi F; Safavi Naini N; Omrani S
    Arch Iran Med; 2014 Jul; 17(7):521-2. PubMed ID: 24979567
    [TBL] [Abstract][Full Text] [Related]  

  • 75. [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]  

  • 76. A rare case of a liveborn with free, de novo and partial trisomy 12 and an unusual phenotype.
    el-Shanti H; Khasawneh M; Hulsberg D; Major H; Patil S
    Ann Genet; 1997; 40(3):175-80. PubMed ID: 9401108
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.
    Tharapel AT; Qumsiyeh MB; Martens PR; Tharapel SA; Dalton JD; Ward JC; Wilroy RS
    Am J Med Genet; 1991 Jul; 40(1):117-20. PubMed ID: 1887840
    [TBL] [Abstract][Full Text] [Related]  

  • 78. "Complete" trisomy 5p; de novo translocation t(2;5)(q36;p11) with isochromosome 5p. Case report and review of the literature.
    Leschot NJ; Lim KS
    Hum Genet; 1979 Feb; 46(3):271-8. PubMed ID: 437770
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Report on 3 patients with 12p duplication including GRIN2B.
    Poirsier C; Landais E; Bednarek N; Nobecourt JM; Khoury M; Schmidt P; Morville P; Gruson N; Clomes S; Michel N; Riot A; Manjeongean C; Gaillard D; Doco-Fenzy M
    Eur J Med Genet; 2014 Apr; 57(5):185-94. PubMed ID: 24503147
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.
    Okada M; Usami A; Okajima K; Yamada M; Yamaguchi Y; Umezaki I; Matsuda Y; Ohta H
    Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.