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Journal Abstract Search

178 related items for PubMed ID: 22354628

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  • 3. Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
    Chen CP, Lin SP, Lin CC, Li YC, Chern SR, Chen WM, Lee CC, Hsieh LJ, Wang W.
    Prenat Diagn; 2005 Feb; 25(2):112-8. PubMed ID: 15712324
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  • 6. A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome.
    Lee JH, Cho HS, Lee ES, Jung BC.
    Korean J Lab Med; 2010 Jun; 30(3):312-7. PubMed ID: 20603594
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  • 11. Direct duplication 16q11.1----16q13 is not associated with a typical dysmorphic syndrome.
    Fryns JP, Kleczkowska A, Decock P, Van den Berghe H.
    Ann Genet; 1990 Jun; 33(1):46-8. PubMed ID: 2195981
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  • 12. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS, Kamel AK, Helmy NA.
    Genet Couns; 2008 Jun; 19(2):199-209. PubMed ID: 18618995
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  • 13. A rare description of pure partial trisomy of 16q12.2q24.3 and review of the literature.
    Manor J, Dinu D, Azamian MS, Bi W, Darilek S, Lalani SR.
    Am J Med Genet A; 2021 Oct; 185(10):2903-2912. PubMed ID: 34061437
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  • 15. Molecular Delineation of Partial Trisomy 14q and Partial Trisomy 12p in a Patient with Dysmorphic Features, Heart Defect and Developmental Delay.
    Bose D, Krishnamurthy V, Venkatesh KS, Aiyaz M, Shetty M, Rao SN, Kutty AV.
    Cytogenet Genome Res; 2015 Oct; 145(1):14-8. PubMed ID: 25896599
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  • 16. [Syndrome of congenital malformations and dysmorphic features in a newborn with partial trisomy 16q due to maternal translocation t(9;16)(p24;q13)].
    Luberda-Zapaśnik J, Midro AT, Szwałkiewicz-Warowicka E.
    Pediatr Pol; 1995 Sep; 70(9):769-73. PubMed ID: 8657511
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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 Sep; 19(4):365-71. PubMed ID: 19239079
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  • 20. Further clinical delineation in trisomy 1q32 syndrome.
    Nuño-Arana I, González-García JR, García-Cruz D.
    Ann Genet; 2001 Sep; 44(4):175-7. PubMed ID: 11755100
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