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 *

107 related articles for article (PubMed ID: 3757308)

  • 1. Comments on methods and results in: Sherman et al., "Segregation analysis of balanced pericentric inversions in pedigree data".
    Stene J
    Clin Genet; 1986 Aug; 30(2):95-107. PubMed ID: 3757308
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Segregation analysis of balanced pericentric inversions in pedigree data.
    Sherman SL; Iselius L; Gallano P; Buckton K; Collyer S; DeMey R; Kristoffersson U; Lindsten J; Mikkelsen M; Morton NE
    Clin Genet; 1986 Aug; 30(2):87-94. PubMed ID: 3757307
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (p11 leads to q13) segment of chromosome 2.
    Baccichetti C; Lenzini E; Peserico A; Tenconi R
    Clin Genet; 1980 Dec; 18(6):402-7. PubMed ID: 7449177
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Pericentric inversions in man. A French collaborative study. Groupe de Cytogénéticiens Français.
    Ann Genet; 1986; 29(3):129-68. PubMed ID: 3538996
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Pericentric inversion of chromosome 12; a three family study.
    Haagerup A; Hertz JM
    Hum Genet; 1992 May; 89(3):292-4. PubMed ID: 1601419
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Monosomy 19pter and trisomy 19q13-qter in two siblings arising from a maternal pericentric inversion: clinical data and molecular characterization.
    Schluth-Bolard C; Till M; Rafat A; Labalme A; Le Lorc'h M; Banquart E; Angei C; Cordier MP; Romana SP; Edery P; Sanlaville D
    Eur J Med Genet; 2008; 51(6):622-30. PubMed ID: 18674648
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ullrich-Turner syndrome (45,X/46,X,i[Xq]) in a child with a familial inversion of chromosome 3.
    Stine SB; Clark CE; Telfer MA; Casey PA; Cowell HR
    Am J Med Genet; 1982 May; 12(1):57-62. PubMed ID: 7091197
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Abnormal chromosome complement resulting from a familial inversion of chromosome 2.
    Richter S; Lockwood B; Lockwood D; Allanson J
    J Med Genet; 1989 Nov; 26(11):725-9. PubMed ID: 2479747
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling.
    Teyssier JR; Bajolle F
    Hum Genet; 1980 Feb; 53(2):195-200. PubMed ID: 7358386
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sperm studies in heterozygote inversion carriers: a review.
    Anton E; Blanco J; Egozcue J; Vidal F
    Cytogenet Genome Res; 2005; 111(3-4):297-304. PubMed ID: 16192708
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Structural differences in pericentric inversions. Application to a model of risk of recombinants.
    Daniel A
    Hum Genet; 1981; 56(3):321-8. PubMed ID: 7239515
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Paracentric inversions in man. A French collaborative study. Groupe de Cytogénéticiens Français.
    Ann Genet; 1986; 29(3):169-76. PubMed ID: 3491573
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial pericentric and paracentric inversions of chromosome 1.
    Johnson DD; Dobyns WB; Gordon H; Dewald GW
    Hum Genet; 1988 Aug; 79(4):315-20. PubMed ID: 3410456
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.