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Journal Abstract Search

569 related items for PubMed ID: 16683276

  • 21. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG, Schuil J, Van Raveswaaij-Arts C, De Pater JM.
    Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
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  • 22. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A, Kitsiou S, Fryssira H, Sofocleous C, Kouvidi E, Tsangaris GT, Salavoura K, Mavrou A.
    In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
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  • 24. Issues arising from the prenatal diagnosis of some rare trisomy mosaics--the importance of cryptic fetal mosaicism.
    Daniel A, Wu Z, Darmanian A, Malafiej P, Tembe V, Peters G, Kennedy C, Adès L.
    Prenat Diagn; 2004 Jul; 24(7):524-36. PubMed ID: 15300743
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  • 25. Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement.
    Pires A, Ramos L, Venâncio M, Rei AI, Castedo S, Saraiva J.
    Prenat Diagn; 2005 Apr; 25(4):292-5. PubMed ID: 15849779
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  • 26. Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism.
    Kosaki R, Hanai S, Kakishima H, Okada MA, Hayashi S, Ito Y, Takahashi T, Kosaki K, Okuyama T.
    Congenit Anom (Kyoto); 2006 Jun; 46(2):115-7. PubMed ID: 16732770
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  • 28. Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literature.
    Redaelli S, Sala E, Roncaglia N, Colombo C, Crosti F, Villa N, Tagliabue P, Cappellini A, Dalprà L.
    Prenat Diagn; 2005 Feb; 25(2):140-7. PubMed ID: 15712378
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  • 29. Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features.
    Kleefstra T, van de Zande G, Merkx G, Mieloo H, Hoovers JM, Smeets D.
    Eur J Hum Genet; 2000 Aug; 8(8):637-40. PubMed ID: 10951526
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  • 30. A phenotypically normal liveborn male after prenatal diagnosis of trisomy 20 mosaicism.
    Von Beust G, Bartels I, Zoll B.
    Genet Couns; 2003 Aug; 14(1):67-74. PubMed ID: 12725591
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  • 31. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.
    Habecker-Green JG, Naeem R, Gold H, O'Grady JP, Kanaan C, Bayer-Zwirello L, Murray MS, Cohn GM.
    J Perinatol; 1998 Aug; 18(5):395-8. PubMed ID: 9766419
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  • 32. Interphase FISH with chromosome-specific protelomere probes for rapid prenatal diagnosis in a reciprocal translocation carrier.
    Cotter PD, Musci TJ.
    Prenat Diagn; 2001 Mar; 21(3):171-5. PubMed ID: 11260602
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  • 34. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22).
    Francisco-Bagnariolli AM, Payão SL, Kawasaki-Oyama RS, Sabbag Filho D, Segato R, de Labio RW, Chauffaille ML, Priest JH.
    Am J Med Genet; 2001 Nov 01; 103(4):302-7. PubMed ID: 11746010
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  • 35. A familial complex chromosome translocation resulting in duplication of 6p25.
    Vermeesch JR, Thoelen R, Fryns JP.
    Ann Genet; 2004 Nov 01; 47(3):275-80. PubMed ID: 15337473
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  • 36. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
    Crowe CA, Schwartz S, Black CJ, Jaswaney V.
    Am J Med Genet; 1997 Sep 05; 71(4):406-13. PubMed ID: 9286446
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  • 37. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
    Koochek M, Harvard C, Hildebrand MJ, Van Allen M, Wingert H, Mickelson E, Holden JJ, Rajcan-Separovic E, Lewis ME.
    Clin Genet; 2006 Feb 05; 69(2):124-34. PubMed ID: 16433693
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  • 38. Prenatal identification of a marker chromosome 16 by chromosome microdissection and reverse FISH.
    de Pater J, Van der Sijs-Bos C, Prins M, Derks J, Albrechts J, Engelen J.
    Eur J Med Genet; 2006 Feb 05; 49(4):306-12. PubMed ID: 16461028
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  • 39. Resolution of trisomic mosaicism in prenatal diagnosis: estimated performance of a 50K SNP microarray.
    Cross J, Peters G, Wu Z, Brohede J, Hannan GN.
    Prenat Diagn; 2007 Dec 05; 27(13):1197-204. PubMed ID: 17994637
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  • 40. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.
    Panasiuk B, Usinskiené R, Kostyk E, Rybałko A, Stasiewicz-Jarocka B, Krzykwa B, Pieńkowska-Grela B, Kucinskas V, Michalova K, Midro AT.
    Ann Genet; 2004 Dec 05; 47(1):11-28. PubMed ID: 15050871
    [Abstract] [Full Text] [Related]

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