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 *

170 related articles for article (PubMed ID: 4043968)

  • 1. Analysis of crossing-over in a family with translocation 9;10 involving a chromosome 9 with a pericentric inversion.
    Priest JH; Lavett DK; Marion JP
    Hum Genet; 1985; 71(2):177-80. PubMed ID: 4043968
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A familial pericentric inversion of chromosome 8 analysed with a high resolution chromosome banding technique.
    Bui TH; Sichong Z; Castro I
    Clin Genet; 1982 Apr; 21(4):266-71. PubMed ID: 7105473
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Pericentric inversion of chromosome 19: prenatal diagnosis and genetic counselling.
    Tharapel AT; Ward JC; Wiggins L; Wilroy RS
    Prenat Diagn; 1986; 6(1):75-8. PubMed ID: 3952060
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal detection of pericentric inversion of chromosome 12.
    Kim HJ; Levy J; Reguero W; Iu B; Wallach RC
    Diagn Gynecol Obstet; 1980; 2(3):231-4. PubMed ID: 7439022
    [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. Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion, inv(8)(p23q22).
    Martin RH
    Cytogenet Cell Genet; 1993; 62(4):199-202. PubMed ID: 8440137
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.
    Levy B; Papenhausen P; Tepperberg J; Dunn T; Fallet S; Magid M; Kardon N; Hirschhorn K; Warburton P
    Cytogenet Cell Genet; 2000; 91(1-4):165-70. PubMed ID: 11173851
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Familial pericentric inversion of chromosome 11 detected prenatally.
    Russell MH; Miller P; Killam A
    J Med Genet; 1982 Apr; 19(2):151-2. PubMed ID: 7077626
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chiasma derived genetic lengths and recombination fractions: a 46, XY, t(9; 10) (p22; q24) reciprocal translocation.
    Laurie DA; Palmer RW; Hultén MA
    Ann Hum Genet; 1985 May; 49(2):135-46. PubMed ID: 4073829
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses.
    Boué A; Gallano P
    Prenat Diagn; 1984; 4 Spec No():45-67. PubMed ID: 6463033
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sperm chromosome analysis in a man heterozygous for a paracentric inversion of chromosome 7 (q11q22).
    Martin RH
    Hum Genet; 1986 Jun; 73(2):97-100. PubMed ID: 3721507
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of balanced chromosome rearrangements in 445 couples with repeated abortion and cytogenetic prenatal testing in carriers.
    Fortuny A; Carrio A; Soler A; Cararach J; Fuster J; Salami C
    Fertil Steril; 1988 May; 49(5):774-9. PubMed ID: 3360167
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Segregation of a complex rearrangement of chromosomes 6, 7, 8, and 12 through three generations.
    Meer B; Wolff G; Back E
    Hum Genet; 1981; 58(2):221-5. PubMed ID: 7197256
    [No Abstract]   [Full Text] [Related]  

  • 18. The offspring of marriage between two first cousins with the same reciprocal translocation t(2;7)(p11;q31).
    Simoni G; Dalprà L; Terzoli GL; Rossella F; Tibiletti MG
    Hum Genet; 1980; 55(2):199-202. PubMed ID: 7192688
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Analysis of synaptonemal complex from a carrier with 46,XY,t(11;18) balanced translocation].
    Liu JY; Wang XR; Zeng XL; Zhang CS; Song YC
    Yi Chuan Xue Bao; 2004 Feb; 31(2):125-31. PubMed ID: 15473301
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The significance of pericentric inversions of chromosome 2.
    Djalali M; Steinbach P; Bullerdiek J; Holmes-Siedle M; Verschraegen-Spae MR; Smith A
    Hum Genet; 1986 Jan; 72(1):32-6. PubMed ID: 3943862
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.