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 *

200 related articles for article (PubMed ID: 12457404)

  • 1. Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.
    Lefort G; Blanchet P; Belgrade N; Rivier F; Chaze AM; Sarda P; Demaille J; Pellestor F
    Am J Med Genet; 2002 Dec; 113(4):333-8. PubMed ID: 12457404
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.
    Lefort G; Blanchet P; Belgrade N; Rivier F; Chaze AM; Sarda P; Demaille J; Pellestor F
    Am J Med Genet A; 2003 Apr; 118A(2):333-8. PubMed ID: 12698965
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Interstitial deletion of 7q31.32 → q33 secondary to a paracentric inversion of a maternal chromosome 7.
    Paskulin GA; Riegel M; Machado Rosa RF; Graziadio C; Gazzola Zen PR
    Eur J Med Genet; 2011; 54(2):181-5. PubMed ID: 21056704
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Recombinant chromosome 18 resulting from a maternal pericentric inversion.
    Ayukawa H; Tsukahara M; Fukuda M; Kondoh O
    Am J Med Genet; 1994 May; 50(4):323-5. PubMed ID: 8209910
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Cytogenetic and molecular genetic study of a case with 8p inverted duplication deletion syndrome].
    Han X; Zhang JM; Jiang WT; Hu Q; Tao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):361-6. PubMed ID: 20677137
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Duplication 19q13-qter and deletion 19p13-pter arising from an inversion (19)(p13.3q13.3) of maternal origin.
    López-Exposito I; Guillén-Navarro E; Bafallíu JA; Bernabé MC; Escalona A; Fuster C
    Eur J Med Genet; 2006; 49(6):511-5. PubMed ID: 16824814
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8.
    Barber JC; James RS; Patch C; Temple IK
    Am J Med Genet; 1994 Apr; 50(3):296-9. PubMed ID: 8042676
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A rec(4) dup 4p inherited from a maternal inv(4)(p15q35): case report and review.
    Garcia-Heras J; Martin J
    Am J Med Genet; 2002 May; 109(3):226-30. PubMed ID: 11977183
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial transmission of a deletion of chromosome 21 derived from a translocation between chromosome 21 and an inverted chromosome 22.
    Aviv H; Lieber C; Yenamandra A; Desposito F
    Am J Med Genet; 1997 Jun; 70(4):399-403. PubMed ID: 9182781
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Reproductive outcomes of paracentric inversion carriers: report of a liveborn dicentric recombinant and literature review.
    Mules EH; Stamberg J
    Hum Genet; 1984; 67(2):126-31. PubMed ID: 6745933
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
    Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
    Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypes.
    Estop AM; Bansal V; Lin A; Levinson F; Karlin SM; Surti U; Wenger SL; Steele MW
    Am J Med Genet; 1994 Feb; 49(4):410-3. PubMed ID: 8160735
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pericentric inversion in human chromosome 8 and spherocytosis.
    Ganguly BB; Dalvi R; Mehta AV
    Cytobios; 2000; 102(400):119-26. PubMed ID: 10885509
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Paracentric inversions of human chromosomes and their risks].
    Balícek P
    Cas Lek Cesk; 2004; 143(1):35-8. PubMed ID: 15061117
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Mother to son transmission of del(1) (q42.1q42.3).
    Sanford Hanna JA; Ball S; Pagon RA; Donlan M
    Am J Med Genet; 2001 Jan; 98(1):103-6. PubMed ID: 11426447
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Paracentric inversion of chromosome 14: a case report.
    Uehara S; Tanigawara S; Takeyama Y; Takabayashi T; Okamura K; Yajima A
    Jpn J Hum Genet; 1994 Sep; 39(3):353-6. PubMed ID: 7841446
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Segregation of inverted chromosome 13 in families ascertained through liveborn recombinant offspring.
    Pai GS; Shields SM; Houser PM
    Am J Med Genet; 1987 May; 27(1):127-33. PubMed ID: 3605191
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.