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 *

92 related articles for article (PubMed ID: 1867252)

  • 1. Unique phenotype associated with a pericentric inversion of chromosome 6 in three generations.
    Wenstrom KD; Muilenburg AC; Patil SR; Hanson JW
    Am J Med Genet; 1991 Apr; 39(1):102-5. PubMed ID: 1867252
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Correlation of the clinical phenotype with a pericentric inversion of chromosome 9].
    Scarinci R; Anichini C; Vivarelli R; Berardi R; Pucci L; Rosaia L; Tomaccini D
    Boll Soc Ital Biol Sper; 1992 Mar; 68(3):175-81. PubMed ID: 1389073
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Pericentric inversion of chromosome 9. Summary of the authors' results].
    Vargas de los Monteros MT; Fernández-Novoa García MC; Salas Herrero E; San Martín Díez MV; Novales Huertas MA
    An Esp Pediatr; 1990 Nov; 33(5):442-9. PubMed ID: 2096758
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pericentric inversion of chromosome 13: familial study and review of the literature.
    Fernández-Novoa C; Vargas T; Fernández-Ortega JM; Gonzalez V; Duenas J
    Genet Couns; 1991; 2(3):133-8. PubMed ID: 1839355
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Clinical implications of chromosomal inversions. A pericentric inversion in No. 18 segregating in a family ascertained through an abnormal proband.
    Martin AO; Simpson JL; Deddish RB; Elias S
    Am J Perinatol; 1983 Oct; 1(1):81-8. PubMed ID: 6680656
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phenotypic variability of Cat-Eye syndrome.
    Berends MJ; Tan-Sindhunata G; Leegte B; van Essen AJ
    Genet Couns; 2001; 12(1):23-34. PubMed ID: 11332976
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Pericentric inversion of a chromosome 21. Study of 3 generations. Genetic counseling].
    Fraisse J
    J Genet Hum; 1975 Oct; 23 SUPPL():107-11. PubMed ID: 129537
    [No Abstract]   [Full Text] [Related]  

  • 10. [Pericentric inversion of the human Y chromosome].
    Motos Guirao MA
    An Esp Pediatr; 1989 Dec; 31(6):583-7. PubMed ID: 2698071
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial pericentric inversion of chromosome 1 (p36.3q23) and Bardet-Biedl syndrome.
    Tayel SM; Al-Naggar RL; Krishna Murthy DS; Naguib KK; Al-Awadi SA
    J Med Genet; 1999 May; 36(5):418-9. PubMed ID: 10353791
    [No Abstract]   [Full Text] [Related]  

  • 12. Congenital anomalies and developmental delay in a boy with double chromosome 6 derived supernumerary marker.
    Oldak M; Waligora J; Gieruszczak-Bialek D; Skorka A; Bocian E; Brycz-Witkowska J; Stankiewicz P; Korniszewski L
    Genet Couns; 2006; 17(1):29-34. PubMed ID: 16719274
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial pericentric inversion of chromosome 2.
    Mattevi MS; Pinheiro CE; Erdtmann B; Flores RZ; Salzano FM
    J Genet Hum; 1981 Jun; 29(2):161-9. PubMed ID: 7328411
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Wolf's syndrome due to pericentric inversion of maternal chromosome 4].
    de la Flor Bru J; Guitart M
    An Esp Pediatr; 1987 Sep; 27(3):205-7. PubMed ID: 3426010
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Maternal pericentric inversion in the origin of an abnormal child due to a recombinant chromosome 1--implications for genetic counseling.
    Pinto MR; Aguiar J; Mota CR
    Genet Couns; 2000; 11(2):179-80. PubMed ID: 10893670
    [No Abstract]   [Full Text] [Related]  

  • 16. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
    Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
    Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5].
    Delozier-Blanchet CD; Pitmon D; Schorderet D; Engel E
    J Genet Hum; 1985 Dec; 33(5):371-80. PubMed ID: 4093767
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multiple congenital anomalies syndrome with myopathy in chromosome 16 abnormality.
    Ionasescu V; Patil S; Hart M; Rhead W; Smith W
    Am J Med Genet; 1987 Jan; 26(1):189-94. PubMed ID: 3812561
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.
    White DM; Pillers DA; Reiss JA; Brown MG; Magenis RE
    Am J Med Genet; 1995 Jul; 57(4):588-97. PubMed ID: 7573135
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Paracentric inversion in the short arm of chromosome 1. Report of a family and review of the literature.
    Cogulu O; Ozkinay F; Gunduz C; Cankaya T; Ozkinay C
    Genet Couns; 2003; 14(4):419-23. PubMed ID: 14738116
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.