BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

246 related articles for article (PubMed ID: 1149493)

  • 1. Cytological assessment of meiotic exchange in a human male with a pericentric inversion of chromosome No. 4.
    Van der Linden AG; Pearson PL; Van de Kamp JJ
    Cytogenet Cell Genet; 1975; 14(2):126-39. PubMed ID: 1149493
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7.
    Winsor EJ; Palmer CG; Ellis PM; Hunter JL; Ferguson-Smith MA
    Cytogenet Cell Genet; 1978; 20(1-6):169-84. PubMed ID: 648176
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Pericentric inversion of chromosome 14 and the risk of partial duplication of 14q (14q31 leads to 14qter).
    Trunca C; Opitz JM
    Am J Med Genet; 1977; 1(2):217-28. PubMed ID: 610431
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18.
    Vianna-Morgante AM; Nozaki MJ; Ortega CC; Coates V; Yamamura Y
    J Med Genet; 1976 Oct; 13(5):366-70. PubMed ID: 1003448
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Duplication deficiency as the result of meiotic segregation of a maternal InV (10).
    Yunis E; Torres de Caballero O
    Hum Genet; 1981; 57(1):71-4. PubMed ID: 7262871
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A complex four-break rearrangement between chromosomes 4 and 13 resulting in a recombinant chromosome 4.
    Andersen O; Lundsteen C; Niebuhr E
    Cytogenet Cell Genet; 1981; 30(1):3-10. PubMed ID: 7261680
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Familial pericentric inversion of chromosome 11 in a child with sporadic unilateral retinoblastoma.
    Ohnishi Y; Shigeto M; Ishibashi T; Hirata J
    Ophthalmic Paediatr Genet; 1990 Dec; 11(4):281-5. PubMed ID: 2096356
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Duplication 11p11.3 leads to 14.1 to meiotic crossing--over.
    Strobel RJ; Riccardi VM; Ledbetter DH; Hittner HM
    Am J Med Genet; 1980; 7(1):15-20. PubMed ID: 7211949
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop.
    Phelan MC; Stevenson RE; Anderson EV
    Am J Med Genet; 1993 May; 46(3):304-8. PubMed ID: 8488876
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Case report of rec(7)dup(7q)inv(7)(p22q22) and a review of the recombinants resulting from parental pericentric inversions on any chromosomes.
    Ishii F; Fujita H; Nagai A; Ogihara T; Kim HS; Okamoto R; Mino M
    Am J Med Genet; 1997 Dec; 73(3):290-5. PubMed ID: 9415687
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Patau's syndrome with D 1 duplication-deficenncy derived from a maternal D group pericentric inversion.
    Parrington JM; Edwards JH
    Ann Hum Genet; 1971 Jul; 35(1):35-45. PubMed ID: 5106368
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. [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]  

  • 16. Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families.
    Boué J; Taillemite JL; Hazael-Massieux P; Léonard C; Boué A
    Humangenetik; 1975 Sep; 30(3):217-24. PubMed ID: 1184007
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Pure trisomy 13q13-qter caused by aneusomic recombination of a maternal pericentric inversion].
    Lucas J; Le Mée F; Picard F; Le Marec B; Junien C
    Ann Genet; 1983; 26(3):187-90. PubMed ID: 6606383
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Duplication-deficiency product of a pericentric inversion in man: a cause of D 1 trisomy syndrome.
    Taysi K; Bobrow M; Balci S; Madan K; Atasu M; Say B
    J Pediatr; 1973 Feb; 82(2):263-8. PubMed ID: 4684369
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. Duplication of 16p from insertion of 16p into 16q with subsequent duplication due to crossing over within the inserted segment.
    Cohen MM; Lerner C; Balkin NE
    Am J Med Genet; 1983 Jan; 14(1):89-96. PubMed ID: 6829613
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.