BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

265 related articles for article (PubMed ID: 22029170)

  • 1. Partial trisomy 14q due to maternal t(4;14)(p16;q32) in a dysmorphic newborn.
    Dundar M; Uzak A; Saatci C; Akalin H
    Genet Couns; 2011; 22(3):287-92. PubMed ID: 22029170
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS; Kamel AK; Helmy NA
    Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
    Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)].
    Turleau C; Grouchy J; Bocquentin F; Roubin M; Colin FC
    Ann Genet; 1975 Mar; 18(1):41-4. PubMed ID: 1080037
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
    Xiao B; Ji X; Jiang WT; Zhang JM; Hu Q; Tao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):654-7. PubMed ID: 22161098
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Partial trisomy 10q: further delineation of the clinical manifestations involving the segment 10q23-->10q24.
    Halpern GJ; Shohat M; Merlob P
    Ann Genet; 1996; 39(3):181-3. PubMed ID: 8839892
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
    Rao VB; Kerketta L; Korgaonkar S; Ghosh K; Mohanty D
    Genet Couns; 2005; 16(2):139-43. PubMed ID: 16082769
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)].
    Raoul O; Rethoré MO; Dutriliaux B; Michon L; Lejeune J
    Ann Genet; 1975 Mar; 18(1):35-9. PubMed ID: 1080036
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature.
    Mishra R; Paththinige CS; Sirisena ND; Nanayakkara S; Kariyawasam UGIU; Dissanayake VHW
    BMC Pediatr; 2018 Jan; 18(1):4. PubMed ID: 29310616
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocation.
    Lukusa T; Devriendt K; Jaeken J; Fryns JP
    Clin Dysmorphol; 1999 Jan; 8(1):47-51. PubMed ID: 10327251
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13).
    Cetin Z; Mihci E; Keser I; Luleci G
    Genet Couns; 2012; 23(2):207-14. PubMed ID: 22876579
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular Delineation of Partial Trisomy 14q and Partial Trisomy 12p in a Patient with Dysmorphic Features, Heart Defect and Developmental Delay.
    Bose D; Krishnamurthy V; Venkatesh KS; Aiyaz M; Shetty M; Rao SN; Kutty AV
    Cytogenet Genome Res; 2015; 145(1):14-8. PubMed ID: 25896599
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Subtelomeric FISH uncovers trisomy 14q32: lessons for imprinted regions, cryptic rearrangements and variant acrocentric short arms.
    Sutton VR; Coveler KJ; Lalani SR; Kashork CD; Shaffer LG
    Am J Med Genet; 2002 Sep; 112(1):23-7. PubMed ID: 12239715
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
    Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
    J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature.
    Paththinige CS; Sirisena ND; Kariyawasam UGIU; Ediriweera RC; Kruszka P; Muenke M; Dissanayake VHW
    BMC Med Genomics; 2018 May; 11(1):44. PubMed ID: 29739404
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.
    Mundhofir FE; Kooper AJ; Winarni TI; Smits AP; Faradz SM; Hamel BC
    Genet Couns; 2010; 21(1):99-108. PubMed ID: 20420036
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
    Cetin Z; Mihci E; Keser I; Karaali K; Berker S; Luleci G
    Genet Couns; 2012; 23(2):239-47. PubMed ID: 22876583
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Syndrome of congenital malformations and dysmorphic features in a newborn with partial trisomy 16q due to maternal translocation t(9;16)(p24;q13)].
    Luberda-Zapaśnik J; Midro AT; Szwałkiewicz-Warowicka E
    Pediatr Pol; 1995 Sep; 70(9):769-73. PubMed ID: 8657511
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocation.
    Kupchik GS; Barrett SK; Babu A; Charria-Ortiz G; Velinov M; Macera MJ
    Eur J Med Genet; 2005; 48(1):57-65. PubMed ID: 15953407
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.