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 *

73 related articles for article (PubMed ID: 3655755)

  • 21. Familial robertsonian translocation 15;21 and rare paracentric inv(21): unexpected re-inversion in a child with translocation trisomy 21.
    Mau UA; Petruch UR; Kaiser P; Eggermann T
    Eur J Hum Genet; 2000 Nov; 8(11):815-9. PubMed ID: 11093270
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mosaic inversion duplication of chromosome 15 without phenotypic effect: occurrence in a father and daughter.
    Knight LA; Lipson M; Mann J; Bachman R
    Am J Med Genet; 1984 Mar; 17(3):649-54. PubMed ID: 6585144
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Acute lymphoblastic leukemia with inv(5)(q13q31) in a pediatric patient.
    de Oliveira FM; Scrideli CA; Queiroz RG; Tone LG
    Cancer Genet Cytogenet; 2006 Feb; 165(1):81-2. PubMed ID: 16490602
    [No Abstract]   [Full Text] [Related]  

  • 24. Homozygosity for pericentric inversions of chromosome 9. Prenatal diagnosis of two cases.
    Cotter PD; Babu A; McCurdy LD; Caggana M; Willner JP; Desnick RJ
    Ann Genet; 1997; 40(4):222-6. PubMed ID: 9526617
    [TBL] [Abstract][Full Text] [Related]  

  • 25. De novo pericentric inversion of chromosome 4, inv(4)(p16q12) in a boy with piebaldism and mental retardation.
    Ramadevi AR; Naik U; Dutta U; Srikanth ; Prabhakara K
    Am J Med Genet; 2002 Nov; 113(2):190-2. PubMed ID: 12407711
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Acquired inv(9): what is its significance?
    Betz JL; Behairy AS; Rabionet P; Tirtorahardjo B; Moore MW; Cotter PD
    Cancer Genet Cytogenet; 2005 Jul; 160(1):76-8. PubMed ID: 15949575
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Periventricular heterotopia in a boy with interstitial deletion of chromosome 4p.
    Gawlik-Kuklinska K; Wierzba J; Wozniak A; Iliszko M; Debiec-Rychter M; Dubaniewicz-Wybieralska M; Limon J
    Eur J Med Genet; 2008; 51(2):165-71. PubMed ID: 18243084
    [TBL] [Abstract][Full Text] [Related]  

  • 28. De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24).
    Jaeken J; Fryns JP; Standaert L; De Cock P; Van den Berghe H
    Ann Genet; 1980; 23(2):105-7. PubMed ID: 6967281
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindred.
    Hirsch B; Baldinger S
    Am J Med Genet; 1993 Jan; 45(1):5-8. PubMed ID: 8418660
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [An anomaly in Poland. A description of a clinical case of a three years and four months-old boy].
    Martino F; Agolini D; Principessa L; Giardini O
    Minerva Pediatr; 1997; 49(1-2):49-52. PubMed ID: 9132560
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
    Battaglia A; Brothman AR; Carey JC
    Am J Med Genet; 2002 Sep; 112(1):103-6. PubMed ID: 12239731
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Tetrasomy 18p: a distinctive syndrome.
    Rivera H; Möller M; Hernández A; Enríquez-Guerra MA; Arreola R; Cantú JM
    Ann Genet; 1984; 27(3):187-9. PubMed ID: 6334486
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literature.
    Hales HA; Peterson CM; Carey J; Hecht BK; Hecht F
    Am J Med Genet; 1993 Nov; 47(6):848-51. PubMed ID: 8279482
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Pericentric inversions of the X chromosome. A new observation and review of the published cases.
    Pfeiffer RA; Kossakiewicz M; Baisch C
    J Genet Hum; 1986 Aug; 34(3-4):331-7. PubMed ID: 3760837
    [TBL] [Abstract][Full Text] [Related]  

  • 35. An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster.
    Vincent JB; Horike SI; Choufani S; Paterson AD; Roberts W; Szatmari P; Weksberg R; Fernandez B; Scherer SW
    J Med Genet; 2006 May; 43(5):429-34. PubMed ID: 16556609
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Unusual chromosome aberrations in 3 children with Down syndrome.
    Osztovics M; Tóth S; Wilhelm O
    Acta Paediatr Acad Sci Hung; 1982; 23(3):283-9. PubMed ID: 6217717
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Recombination aneusomy of subtelomeric regions of chromosome 5, resulting from a large familial pericentric inversion inv(5)(p15.33q35.3).
    Bocian E; Suchenek K; Obersztyn E; Nowakowska B; Mazurczak T
    J Appl Genet; 2005; 46(1):109-14. PubMed ID: 15741672
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies.
    Celep F; Acar H; Aynaci O; Aynaci FM; Karagüzel A
    Genet Couns; 2001; 12(4):319-26. PubMed ID: 11837600
    [TBL] [Abstract][Full Text] [Related]  

  • 40. High recurrence of recombinants in a family with pericentric inversion of chromosome 18.
    Mejía-Baltodano G; Bobadilla L; Gonzalez RM; Barros-Núñez P
    Ann Genet; 1997; 40(3):164-8. PubMed ID: 9401106
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.