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 *

180 related articles for article (PubMed ID: 3184143)

  • 1. Trisomy 3p23----pter and monosomy 11q23----qter in an infant with two translocation carrier parents.
    Neu RL; Kousseff BG; Hardy DE; Essig YP; Miller KL; Jervis GA; Tedesco TA
    J Med Genet; 1988 Sep; 25(9):631-3. PubMed ID: 3184143
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of a derivative chromosome 17 by fish-technique.
    Ramesh KH; Shah HO; Sherman J; Lin JH; Verma RS
    Ann Genet; 1996; 39(3):177-80. PubMed ID: 8839891
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Phenotypic and genetic analysis of a boy with 3p26.3-pter deletion and 7q31.33-qter duplication].
    Feng L; Cai W; Jiang J; Sun S; Jing C; Yuan L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):535-539. PubMed ID: 30098251
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
    Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY
    Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement.
    Preiksaitiene E; Benušienė E; Ciuladaite Z; Šliužas V; Mikštienė V; Kučinskas V
    Taiwan J Obstet Gynecol; 2016 Jun; 55(3):410-4. PubMed ID: 27343325
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.
    Cervantes A; García-Delgado C; Fernández-Ramírez F; Galaz-Montoya C; Morales-Jiménez AB; Nieto-Martínez K; Gómez-Laguna L; Villa-Morales J; Quintana-Palma M; Berúmen J; Kofman S; Morán-Barroso VF
    BMC Med Genomics; 2014 Sep; 7():55. PubMed ID: 25223409
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial monosomy 13q and partial trisomy 18p: case report with necropsy findings.
    Beneck D; Greco MA; Wolman SR; McMorrow LE; Jansen V; Cason J
    J Med Genet; 1986 Jun; 23(3):260-3. PubMed ID: 3723557
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
    Balci S; Aypar E; Beksaç MS; Bartsch O
    Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial trisomy 2q(2q37.3-->qter) and monosomy 7q(7q34--->qter) due to paternal reciprocal translocation 2;7: a case report.
    Ahn JM; Koo DH; Kwon KW; Lee YK; Lee YH; Lee HH; Nam KH; Lee KH
    J Korean Med Sci; 2003 Feb; 18(1):112-3. PubMed ID: 12589098
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Monosomy 10q26-qter and trisomy 11q13-qter as a result of de novo unbalanced translocation.
    Tinsa F; Chebbi Y; Meddeb M; Bousnina D; Boussetta K; Bousnina S
    J Appl Genet; 2009; 50(3):289-91. PubMed ID: 19638686
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3).
    Asano T; Ikeuchi T; Shinohara T; Enokido H; Hashimoto K
    Jinrui Idengaku Zasshi; 1991 Sep; 36(3):257-65. PubMed ID: 1753439
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial trisomy 2p24-->pter and monosomy 18q22.1- qter resulting from parental translocation.
    Atik T; Durmaz B; Yorganci OU; Cogulu O; Kioutsouk M; Ozkinay F
    Genet Couns; 2013; 24(2):179-84. PubMed ID: 24032288
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter).
    Lukusa T; Devriendt K; Fryns JP
    Ann Genet; 1999; 42(2):91-4. PubMed ID: 10434122
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Wolf-Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter.
    Iwanowski PS; Panasiuk B; Van Buggenhout G; Murdolo M; Myśliwiec M; Maas NM; Lattante S; Korniszewski L; Posmyk R; Pilch J; Zajączek S; Fryns JP; Zollino M; Midro AT
    Am J Med Genet A; 2011 Aug; 155A(8):1833-47. PubMed ID: 21744486
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fetal phenotype in a case of partial trisomy 21 and partial monosomy 22 detected prenatally.
    Migliorini AM; Coco R; De Negrotti TC; Sanchez JM; Castineyra G
    J Med Genet; 1981 Oct; 18(5):383-5. PubMed ID: 6460105
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
    Schimmenti LA; Higgins RR; Mendelsohn NJ; Casey TM; Steinberger J; Mammel MC; Wiesner GL
    Am J Med Genet; 1995 May; 57(1):52-6. PubMed ID: 7645598
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Partial trisomy 3q syndrome inherited from familial t(3;9)(q26.1; p23).
    Tranebjaerg L; Baekmark UB; Dyhr-Nielsen M; Kreiborg S
    Clin Genet; 1987 Aug; 32(2):137-43. PubMed ID: 3652493
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial trisomy 3p and partial monosomy 11q associated with double outlet right ventricle and septum pellucidum et vergae: a case report.
    Say B; Guzoglu N; Uras N; Candemir Z; Akin I; Dilmen U
    Genet Couns; 2013; 24(4):387-91. PubMed ID: 24551981
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Trisomy 2q and monosomy 11q in the same individual: the importance of considering the deleted segment.
    Ardinger HH; Patil SR; Rhead WJ
    Clin Genet; 1987 Jun; 31(6):381-5. PubMed ID: 3621640
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.