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Journal Abstract Search

220 related items for PubMed ID: 610431

  • 1. 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
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  • 3. 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
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  • 8. 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
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  • 12. [Severe mental retardation and slight dysmorphism in a child with a bisatellite extrachromosome: inversion duplication (15)?].
    Rinaldi MM, Militerni R, Pascotto A, Scarano G, Renda S, Cavaliere ML, Santulli B, Esposito M, Ventruto V.
    Pediatr Med Chir; 1982 Oct; 4(5):559-61. PubMed ID: 6927358
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  • 13. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A, Lapunzina P, Palomares M, Molina MA, Galán E, López Pajares I.
    Eur J Med Genet; 2005 Oct; 48(2):159-66. PubMed ID: 16053907
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  • 14. Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin.
    Lacbawan FL, White BJ, Anguiano A, Rigdon DT, Ball KD, Bromage GB, Yang X, DiFazio MP, Levin SW.
    Am J Med Genet; 1999 Nov 19; 87(2):139-42. PubMed ID: 10533028
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  • 17. Inherited parital duplication deficiency of chromosome 15 (p12;q22).
    Coco R, Penchaszadeh VB.
    J Genet Hum; 1978 Sep 19; 26(3):203-10. PubMed ID: 739260
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  • 20. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
    Battaglia A, Brothman AR, Carey JC.
    Am J Med Genet; 2002 Sep 15; 112(1):103-6. PubMed ID: 12239731
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