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Journal Abstract Search

261 related items for PubMed ID: 12457409

  • 21. Mosaic trisomy 14 with hepatic involvement.
    Iglesias A, McCurdy LD, Glass IA, Cotter PD, Illueca M, Perenyi A, Sansaricq C.
    Ann Genet; 1997; 40(2):104-8. PubMed ID: 9259957
    [Abstract] [Full Text] [Related]

  • 22. Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.
    Dawson AJ, Mears AJ, Chudley AE, Bech-Hansen T, McDermid H.
    J Med Genet; 1996 Nov; 33(11):952-6. PubMed ID: 8950677
    [Abstract] [Full Text] [Related]

  • 23. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS, Kamel AK, Helmy NA.
    Genet Couns; 2008 Nov; 19(2):199-209. PubMed ID: 18618995
    [Abstract] [Full Text] [Related]

  • 24. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
    Lassota M, Przełozna B, Płodzien M, Bugno M, Wnuk M, Kotylak Z, Słota E.
    J Appl Genet; 2005 Nov; 46(4):419-21. PubMed ID: 16278518
    [Abstract] [Full Text] [Related]

  • 25. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
    Lorentz CP, Jalal SM, Thompson DM, Babovic-Vuksanovic D.
    Am J Med Genet; 2002 Jul 22; 111(1):61-7. PubMed ID: 12124737
    [Abstract] [Full Text] [Related]

  • 26. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B, Hacihanefioglu S, Silahtaroglu A, Yilmaz S, Deviren A, Cenani A.
    Genet Couns; 2000 Jul 22; 11(4):355-61. PubMed ID: 11140413
    [Abstract] [Full Text] [Related]

  • 27. Abnormal chromosome 9 in a neonate program. Report of three cases.
    Nakamura Y, Sato E, Sakai K, Sakuma S, Hashimoto T, Sindou S.
    Arch Pathol Lab Med; 1990 Feb 22; 114(2):185-7. PubMed ID: 2302035
    [Abstract] [Full Text] [Related]

  • 28. Trisomy 9p syndrome in two brothers: with new clinical findings and review of the literature.
    Hacihanefioğlu S, Güven GS, Deviren A, Silahtaroğlu AN, Yosunvkaya Fenerci E, Ozkiliç A, Yüksel A.
    Genet Couns; 2002 Feb 22; 13(1):41-8. PubMed ID: 12017237
    [Abstract] [Full Text] [Related]

  • 29. Unbalanced mosaic karyotypes with different structural abnormalities involving a common chromosome region: report of two cases.
    Pettenati MJ, Teot LA, Smith C, Hayworth R, Thomas IT, Veille JC, Rao PN.
    Am J Med Genet; 1993 Feb 01; 45(3):365-9. PubMed ID: 8434625
    [Abstract] [Full Text] [Related]

  • 30. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
    Grammatico P, Majore S, Marrocco G, Poscente M, Mordenti C, Grammatico B, Del Porto G.
    Genet Couns; 1999 Feb 01; 10(4):351-8. PubMed ID: 10631922
    [Abstract] [Full Text] [Related]

  • 31. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
    Wouters CH, van Bodegom TM, Moll HA, Govaerts LC.
    Ann Genet; 1999 Feb 01; 42(3):160-5. PubMed ID: 10526659
    [Abstract] [Full Text] [Related]

  • 32. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
    Oner G, Jauch A, Eggermann T, Hardwick R, Kirsch S, Schiebel K, Rappold G, Robson L, Smith A.
    Am J Med Genet; 2000 May 15; 92(2):101-6. PubMed ID: 10797432
    [Abstract] [Full Text] [Related]

  • 33. Partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages.
    Demirhan O, Tastemir D.
    Fertil Steril; 2006 Jul 15; 86(1):219.e15-9. PubMed ID: 16818035
    [Abstract] [Full Text] [Related]

  • 34. Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies.
    Celep F, Acar H, Aynaci O, Aynaci FM, Karagüzel A.
    Genet Couns; 2001 Jul 15; 12(4):319-26. PubMed ID: 11837600
    [Abstract] [Full Text] [Related]

  • 35. Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis.
    Prontera P, Buldrini B, Aiello V, Gruppioni R, Bonfatti A, Venti G, Ferlini A, Sensi A, Calzolari E, Donti E.
    Prenat Diagn; 2006 Jun 15; 26(6):571-6. PubMed ID: 16683276
    [Abstract] [Full Text] [Related]

  • 36. Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype.
    Wieczorek D, Prott EC, Robinson WP, Passarge E, Gillessen-Kaesbach G.
    Prenat Diagn; 2003 Feb 15; 23(2):128-33. PubMed ID: 12575019
    [Abstract] [Full Text] [Related]

  • 37. Wolf-Hirschhorn syndrome owing to 1:3 segregation of a maternal 4;21 translocation.
    Bauer K, Howard-Peebles PN, Keele D, Friedman JM.
    Am J Med Genet; 1985 Jun 15; 21(2):351-6. PubMed ID: 4014316
    [Abstract] [Full Text] [Related]

  • 38. Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother.
    Fujimoto A, Lin MS, Korula SR, Wilson MG.
    Am J Med Genet; 1985 Oct 15; 22(2):333-42. PubMed ID: 4050866
    [Abstract] [Full Text] [Related]

  • 39. Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocation.
    Frints SG, Moerman P, Fryns JP.
    Genet Couns; 1996 Oct 15; 7(4):313-9. PubMed ID: 8985736
    [Abstract] [Full Text] [Related]

  • 40. Trisomy 21 mosaicism in two subjects from two generations.
    Casati A, Giorgi R, Lanza A, Raimondi E, Vagnarelli P, Mondello C, Ghetti P, Piazzi G, Nuzzo F.
    Ann Genet; 1992 Oct 15; 35(4):245-50. PubMed ID: 1296525
    [Abstract] [Full Text] [Related]

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