BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 6212612)

  • 1. The clinical significance of pericentric inversion of the human Y chromosome: a rare "third" type of heteromorphism.
    Verma RS; Rodriguez J; Dosik H
    J Hered; 1982; 73(3):236-8. PubMed ID: 6212612
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. Pericentric inversion of the Y chromosome of infertile male.
    Tomomasa H; Adachi Y; Iwabuchi M; Oshio S; Umeda T; Iino Y; Takano T; Nakahori Y
    Arch Androl; 2000; 45(3):181-5. PubMed ID: 11111866
    [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. Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 20.
    Jenderny J; Gebauer J; Röhrborn G; Rüger A
    Hum Genet; 1992 Apr; 89(1):117-9. PubMed ID: 1577458
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inherited pericentric inversion of Y-chromosome with trisomy 21. A case report.
    Krishna Murthy DS; Murthy SK; Patel JK; Banker GN; Shah VC
    Ann Genet; 1989; 32(1):47-51. PubMed ID: 2526612
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion.
    Shashi V; Golden WL; Allinson PS; Blanton SH; von Kap-Herr C; Kelly TE
    Am J Hum Genet; 1996 Jun; 58(6):1231-8. PubMed ID: 8651300
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pericentric inversion of the Y chromosome and prenatal diagnosis.
    Shapiro LR; Pettersen RO; Wilmot PL; Warburton D; Benn PA; Hsu LY
    Prenat Diagn; 1984; 4(6):463-5. PubMed ID: 6522349
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interchromosomal effect leading to an increase in aneuploidy in sperm nuclei in a man heterozygous for pericentric inversion (inv 9) and C-heterochromatin.
    Amiel A; Sardos-Albertini F; Fejgin MD; Sharony R; Diukman R; Bartoov B
    J Hum Genet; 2001; 46(5):245-50. PubMed ID: 11355013
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Turner's syndrome with a duplication-deficiency X chromosome derived from a maternal pericentric inversion X chromosome.
    Maeda T; Ohno M; Takada M; Nishida M; Tsukioka K; Tomita H
    Clin Genet; 1979 Mar; 15(3):259-66. PubMed ID: 421365
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Unusual segregation products in sperm from a pericentric inversion 17 heterozygote.
    Mikhaail-Philips MM; McGillivray BC; Hamilton SJ; Ko E; Chernos J; Rademaker A; Martin RH
    Hum Genet; 2005 Aug; 117(4):357-65. PubMed ID: 15924233
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [Pericentric inversion of the Y chromosome as an exclusion constellation].
    Bullerdiek J; Bartnitzke S; Pahlke R
    Anthropol Anz; 1984 Mar; 42(1):67-72. PubMed ID: 6586109
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1.
    Martin RH; Chernos JE; Lowry RB; Pattinson HA; Barclay L; Ko E
    Hum Genet; 1994 Feb; 93(2):135-8. PubMed ID: 8112736
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Double trisomy and transmitted pericentric inversion (48,XXY, +21,inv(22)). Interchromosomal effect].
    Saura R; Longy M; Sautarael M; Renouil M; Sandler B
    Ann Genet; 1983; 26(3):180-2. PubMed ID: 6606381
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Coexistence of inverted Y, chromosome 15p+ and abnormal phenotype.
    Acar H; Cora T; Erkul I
    Genet Couns; 1999; 10(2):163-70. PubMed ID: 10422010
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The inverted Y-chromosome polymorphism in the Gujarati Muslim Indian population of South Africa has a single origin.
    Spurdle A; Jenkins T
    Hum Hered; 1992; 42(5):330-2. PubMed ID: 1459580
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial pericentric inversion of the Y chromosome.
    Tóth A; Gaál M; László J
    Ann Genet; 1984; 27(1):60-1. PubMed ID: 6609677
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Familial pericentric inversion of the X chromosome [inv(X)(p11q28)]].
    Baumann W; Zabel B; Holl M
    Ann Genet; 1984; 27(2):106-8. PubMed ID: 6331785
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of partial trisomy 21 associated with maternal balanced translocation 46xx der 21 t(21q;22q) with pericentric inversion of chromosome 9.
    Parmar RC; Sira P
    J Postgrad Med; 2003; 49(2):154-6. PubMed ID: 12867693
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.