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 *

214 related articles for article (PubMed ID: 7438504)

  • 1. Trisomy 18q: 46,XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46,XY,-13,+der(13),t(13;18)(q32;q11).
    Murthy DS; Patel ZM; Ambani LM
    Clin Genet; 1980 Oct; 18(4):233-8. PubMed ID: 7438504
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial trisomy 18(q11 leads to qter) in an infant and aborted fetus resulting from a balanced paternal translocation t(13;18)(q32:q11).
    Rosenmann A; Isacson M; Cohen R; Segal M; Cohen MM
    Ann Genet; 1978 Mar; 21(1):60-4. PubMed ID: 308346
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Maternal translocation t(13:18)(q34:q11) and Edward's syndrome in a fetus: 47,xy,t(13:18)(q34:q11) + 18.
    Marković S; Boué J; Krstić M; Sulović V; Dozić S; Adzić S
    Clin Genet; 1984 Nov; 26(5):481-4. PubMed ID: 6499261
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Trisomy 18q: 46,XX,-10,+der(10) t(10;18) (p15;q12) pat: a case report.
    Murthy SK; Kar B; Prabhakara K; Krishnamurthy DS
    Ann Genet; 1992; 35(3):174-7. PubMed ID: 1466569
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat.
    Stern LM; Mureh AR
    J Med Genet; 1975 Sep; 12(3):305-7. PubMed ID: 1177285
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Tertiary trisomy, 47,XX,+14q--, resulting from maternal balanced translocation, 46,XX,t(14;16)(q11;q24).
    Young SR; Donovan DM; Greer HA; Burch K; Potter DC
    Hum Genet; 1976 Aug; 33(3):331-4. PubMed ID: 964994
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Partial trisomy 13q inherited from balanced translocation (5;13) (p14;q13).
    Coco R; del Rey G
    J Genet Hum; 1978 Dec; 26(4):303-10. PubMed ID: 752064
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trisomy 4p and partial monosomy 18q due to paternal translocation t(4;18) (p11; q21.3).
    Thanemozhi G; Santhiya ST; Chandra N; Palka G; Jayam S; Gopinath PM
    Indian J Pediatr; 2000 Aug; 67(8):601-4. PubMed ID: 10985005
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A child with partial trisomy of chromosome 17 and partial monosomy of chromosome 3: 46,XY,der(3),t(3;17)(p25;q23).
    Shawe DJ; Fear C; Appleyard WJ
    J Med Genet; 1983 Oct; 20(5):383-5. PubMed ID: 6196484
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature.
    Duckett DP; Roberts SH
    Hum Genet; 1981; 58(4):377-86. PubMed ID: 7035334
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation.
    Hou JW
    Chang Gung Med J; 2003 Jan; 26(1):48-52. PubMed ID: 12656309
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. Two reciprocal translocations t(9p+;13q-) and t(13q-;21q+): a study of the families.
    Prieto F; Badia L; Asensi F; Roques V
    Hum Genet; 1980; 54(1):7-11. PubMed ID: 7390483
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fatal Outcome in a Newborn Calf Associated with Partial Trisomy 25q and Partial Monosomy 11q, 60,XX,der(11)t(11;25)(q11;q14∼21).
    Iannuzzi A; Genualdo V; Perucatti A; Pauciullo A; Varricchio G; Incarnato D; Matassino D; Iannuzzi L
    Cytogenet Genome Res; 2015; 146(3):222-9. PubMed ID: 26337016
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Partial trisomy 16p due to maternal balanced translocation.
    McMorrow LE; Bornstein S; Fischer RH; Gluckson MM
    J Med Genet; 1984 Aug; 21(4):315-6. PubMed ID: 6492098
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Trisomy 16q arising from a maternal 15p;16q translocation.
    Ridler MA; McKeown JA
    J Med Genet; 1979 Aug; 16(4):317-20. PubMed ID: 490587
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.