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Journal Abstract Search

137 related items for PubMed ID: 1519645

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  • 3. A new case of a severe clinical phenotype of the cat-eye syndrome.
    Denavit TM, Malan V, Grillon C, Sanlaville D, Ardalan A, Jacquemont ML, Burglen L, Taillemite JL, Portnoi MF.
    Genet Couns; 2004; 15(4):443-8. PubMed ID: 15658620
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  • 4. Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
    Klein OD, Cotter PD, Albertson DG, Pinkel D, Tidyman WE, Moore MW, Rauen KA.
    Clin Genet; 2004 Jun; 65(6):477-82. PubMed ID: 15151506
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  • 10. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
    Cai T, Yu P, Tagle DA, Xia J.
    Am J Med Genet; 1999 Oct 08; 86(4):305-11. PubMed ID: 10494083
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  • 13. Digeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literature.
    Dallapiccola B, Marino B, Giannotti A, Valorani G.
    Ann Genet; 1989 Oct 08; 32(2):92-6. PubMed ID: 2667458
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  • 14. Duplication of distal 22q.
    Abeliovich D, Maor E, Bashan N, Carmi R.
    Am J Med Genet; 1989 Mar 08; 32(3):346-9. PubMed ID: 2729354
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  • 15. Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.
    Knoll JH, Asamoah A, Pletcher BA, Wagstaff J.
    Am J Med Genet; 1995 Jan 16; 55(2):221-4. PubMed ID: 7717422
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  • 16. A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype.
    Park JP, McDermet MK, Moeschler JB, Wurster-Hill DH.
    Ann Genet; 1993 Jan 16; 36(4):217-20. PubMed ID: 8166428
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  • 18. Unbalanced translocation (15;17)(q13;13.3) with apparent Prader-Willi syndrome but without Miller-Dieker syndrome.
    Elder FF, Nichols MM, Hood OJ, Harrison WR.
    Am J Med Genet; 1985 Mar 16; 20(3):519-24. PubMed ID: 3993677
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  • 19. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
    de Ravel T, Aerssens P, Vermeesch JR, Fryns JP.
    Eur J Med Genet; 2005 Mar 16; 48(3):355-9. PubMed ID: 16179232
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  • 20. Deletions of proximal 15q without Prader-Willi syndrome.
    Greenberg F, Ledbetter DH.
    Am J Med Genet; 1987 Dec 16; 28(4):813-20. PubMed ID: 3688019
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