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Journal Abstract Search

225 related items for PubMed ID: 7246613

  • 1. Duplication 3p syndrome: report of a new case and review of the literature.
    Charrow J, Cohen MM, Meeker D.
    Am J Med Genet; 1981; 8(4):431-6. PubMed ID: 7246613
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  • 2. Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family.
    de Pina Neto JM, Ferrari I.
    Am J Med Genet; 1980; 5(1):25-33. PubMed ID: 7395898
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  • 4. The phenotypic and cytogenetic spectrum of partial trisomy 9.
    Wilson GN, Raj A, Baker D.
    Am J Med Genet; 1985 Feb; 20(2):277-82. PubMed ID: 3976721
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  • 5. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P, Adkins WN, Caspar H, Dumars KW, Gebauer J, Gilbert EF, Grimm T, Habedank M, Hansmann I, Herrmann J, Kaveggia EG, Langenbeck U, Meisner LF, Najafzadeh TM, Opitz JM, Palmer CG, Peters HH, Scholz W, Tavares AS, Wiedeking C.
    Am J Med Genet; 1981 Feb; 10(2):159-77. PubMed ID: 7315873
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  • 7. Trisomy 14 mosaicism: case report and review.
    Johnson VP, Aceto T, Likness C.
    Am J Med Genet; 1979 Feb; 3(4):331-9. PubMed ID: 474633
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  • 8. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
    Schimmenti LA, Higgins RR, Mendelsohn NJ, Casey TM, Steinberger J, Mammel MC, Wiesner GL.
    Am J Med Genet; 1995 May 22; 57(1):52-6. PubMed ID: 7645598
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  • 9. Duplication 6q24 leads to 6qter in an infant from a balanced paternal translocation.
    Chase TR, Jalal SM, Martsolf JT, Wasdahl WA.
    Am J Med Genet; 1983 Feb 22; 14(2):347-51. PubMed ID: 6837629
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  • 11. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
    van Buggenhout G, Decock P, Fryns JP.
    Genet Couns; 1996 Feb 22; 7(1):53-9. PubMed ID: 8652089
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  • 14. Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22).
    Bowen P, Fitzgerald PH, Gardner RJ, Biederman B, Veale AM.
    Am J Med Genet; 1983 Apr 22; 14(4):635-46. PubMed ID: 6846399
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  • 17. Complete trisomy 17p a relatively new syndrome.
    Martsolf JT, Larson L, Jalal SM, Wasdahl WA, Miller R, Kukolich M.
    Ann Genet; 1988 Apr 22; 31(3):172-4. PubMed ID: 3066280
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  • 18. Duplication 6q syndrome.
    Tipton RE, Berns JS, Johnson WE, Wilroy RS, Summitt RL.
    Am J Med Genet; 1979 Apr 22; 3(4):325-30. PubMed ID: 474632
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  • 19. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H, Vermeesch J, Fryns JP.
    Genet Couns; 2008 Apr 22; 19(4):365-71. PubMed ID: 19239079
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