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Journal Abstract Search

168 related items for PubMed ID: 3919583

  • 1.
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  • 2. The dup(3)(p25 leads to pter) syndrome: a case with holoprosencephaly.
    Martin NJ, Steinberg BG.
    Am J Med Genet; 1983 Apr; 14(4):767-72. PubMed ID: 6846406
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  • 3. Cyclopia and cebocephaly in two newborn infants with unbalanced segregation of a familial translocation rcp (1;7)(q32;q34).
    Schinzel A.
    Am J Med Genet; 1984 May; 18(1):153-61. PubMed ID: 6430085
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  • 4. Partial duplication for the short arm of chromosome 2 : the 2p23 to pter syndrome.
    Rosenfeld W, Verma RS, Jhaveri R, Dosik H, Evans H.
    Ann Genet; 1982 May; 25(1):28-31. PubMed ID: 6979296
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  • 5. Duplication of distal 22q.
    Abeliovich D, Maor E, Bashan N, Carmi R.
    Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
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  • 6. Duplication (5p13 leads to pter): prenatal diagnosis and review of the literature.
    Khodr GS, Cadena G, Le KL, Kagan-Hallet KS.
    Am J Med Genet; 1982 May; 12(1):43-9. PubMed ID: 7091195
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  • 9. Partial 3q trisomy due to an unbalanced 3/10 translocation.
    Blumberg B, Moore R, Mohandas T.
    Am J Med Genet; 1980 May; 7(3):335-9. PubMed ID: 7468658
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  • 10. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
    Chen CP, Devriendt K, Lee CC, Chen WL, Wang W, Wang TY.
    Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
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  • 11. Partial duplication 16p resulting from a 3:1 segregation of a maternal reciprocal translocation.
    Mori MA, Gomar JL, Diaz de Bustamante A, Ananias A, Pinel I, Martinez-Frias ML.
    Am J Med Genet; 1987 Jan; 26(1):203-6. PubMed ID: 3812563
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  • 12. Prenatal diagnosis of a dup(3p) with holoprosencephaly.
    Gillerot Y, Hustin J, Koulischer L, Viteux V.
    Am J Med Genet; 1987 Jan; 26(1):225-7. PubMed ID: 3812567
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  • 13. Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12).
    Gonzalez CH, Billerbeck AE, Takayama LC, Wajntal A.
    Am J Med Genet; 1983 Jan; 14(1):159-67. PubMed ID: 6829605
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  • 16. Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2.
    Pivnick EK, Wilroy RS, Summitt JB, Tucker B, Herrod HG, Tharapel AT.
    Am J Med Genet; 1990 Sep; 37(1):92-6. PubMed ID: 2240050
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  • 17. Brief cytogenetic report on maternal translocation t(7;9) (p22:p13): two sibs with duplication 9p and one sib with the balanced translocation.
    Wajntal A, Gonzalez CH, Koiffmann CP, de Souza DH.
    Am J Med Genet; 1985 Feb; 20(2):265-9. PubMed ID: 3976719
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  • 19. 8q22-->qter duplication in a child with multiple congenital malformations: case report.
    Sasiadek M, Stembalska A, Schlade K, Zych M.
    Med Sci Monit; 2000 Feb; 6(1):141-4. PubMed ID: 11208302
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