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 *

149 related articles for article (PubMed ID: 6716417)

  • 1. Familial pericentric inversion (13) detected by antenatal diagnosis.
    Maltby EL
    J Med Genet; 1984 Apr; 21(2):149-51. PubMed ID: 6716417
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A fetus with recombinant of chromosome 8 inherited from her carrier father.
    Fujimoto A; Towner JW; Turkel SB; Wilson MG
    Hum Genet; 1978 Feb; 40(3):241-8. PubMed ID: 631845
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
    Chen CP; Ko TM; Su YN; Wang LK; Chern SR; Wu PS; Chen YN; Chen SW; Ko K; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):733-737. PubMed ID: 27751426
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pericentric inversion (13) with two different recombinants in the same family.
    Williamson EM; Miller JF; Seabright M
    J Med Genet; 1980 Aug; 17(4):309-12. PubMed ID: 7205907
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal exclusion of segmental trisomy in familial chromosome 21 pericentric inversion by fluorescence in situ hybridization.
    Tardy EP; Tóth A; Kosztolányi G
    Prenat Diagn; 1997 Sep; 17(9):871-3. PubMed ID: 9316133
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recombinant chromosome 18 in two offspring of a chromosome 18 inversion heterozygote.
    Andrews T; Gardiner AC; Boon AR
    Ann Genet; 1982; 25(3):185-8. PubMed ID: 6982674
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Peri- and paracentric inversions in chromosome 12: prenatal diagnosis and family study.
    Poulsen H; Mikkelsen M; Holmgren G
    Prenat Diagn; 1981 Jan; 1(1):35-42. PubMed ID: 7346810
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers.
    Sutherland GR; Gardiner AJ; Carter RF
    Clin Genet; 1976 Jul; 10(1):54-9. PubMed ID: 949865
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial inversion of chromosome No. 8: an affected child and a carrier fetus.
    Fujimoto A; Wilson MG; Towner JW
    Humangenetik; 1975; 27(1):67-73. PubMed ID: 49288
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Relatives with opposite chromosome constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a familial pericentric inversion.
    Ciuladaite Z; Preiksaitiene E; Utkus A; Kučinskas V
    Cytogenet Genome Res; 2014; 144(2):109-13. PubMed ID: 25401700
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.
    Daniel A; Hook EB; Wulf G
    Am J Med Genet; 1989 May; 33(1):14-53. PubMed ID: 2750783
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The prenatal detection of a familial pericentric inversion of chromosome 19.
    Couzin DA; Watt JL; Stephen GS
    Prenat Diagn; 1986; 6(1):79-82. PubMed ID: 3952061
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Cytogenetic study of a case of Fanconi's syndrome with a familial pericentric inversion].
    Crippa L; Ferrier S
    J Genet Hum; 1975 Mar; 23(1):7-16. PubMed ID: 1165481
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Paracentric inversion inv(11)(q21q23) in The Netherlands.
    Madan K; Pieters MH; Kuyt LP; van Asperen CJ; de Pater JM; Hamers AJ; Gerssen-Schoorl KB; Hustinx TW; Breed AS; Van Hemel JO
    Hum Genet; 1990 Jun; 85(1):15-20. PubMed ID: 2358301
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysis.
    Martin AO; Northrup H; Ledbetter DH; Trask B; van den Engh G; Le Beau MM; Beaudet AL; Gray JW; Sekhon G; Krassikoff N
    Am J Med Genet; 1988 Nov; 31(3):643-54. PubMed ID: 3228143
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial pericentric inversion of chromosome 12.
    Voiculescu I; Barbi G; Wolff G; Steinbach P; Back E; Schempp W
    Hum Genet; 1986 Apr; 72(4):320-2. PubMed ID: 3699821
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Three large Danish families with a paracentric inversion in the short arm of chromosome N. 5.
    Baggesen K; Friedrich U; Jensen PK; Rasmussen K
    Ann Genet; 1988; 31(1):50-2. PubMed ID: 3258494
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [Pericentric inversion of human chromosomes and its risks] ].
    Balícek P
    Cas Lek Cesk; 2001 Feb; 140(2):38-42. PubMed ID: 11262905
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.