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Journal Abstract Search

240 related items for PubMed ID: 11438955

  • 41. Fetal cells in cervical mucus in the first trimester of pregnancy.
    Cioni R, Bussani C, Scarselli B, Bucciantini S, Barciulli F, Scarselli G.
    Prenat Diagn; 2003 Feb; 23(2):168-71. PubMed ID: 12575028
    [Abstract] [Full Text] [Related]

  • 42. Comparison of two techniques for transcervical cell sampling performed in the same study population.
    Cioni R, Bussani C, Scarselli B, Bucciantini S, Marchionni M, Scarselli G.
    Prenat Diagn; 2005 Mar; 25(3):198-202. PubMed ID: 15791667
    [Abstract] [Full Text] [Related]

  • 43. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
    Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ.
    Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
    [Abstract] [Full Text] [Related]

  • 44. [Using multiplex PCR to analyze the breakpoint of a severe Y-chromosome deletion].
    Xiao XS, Liu XY, Wang YQ, Zhou Y, Ouyang L, Zhang X, Cai ZM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Oct; 22(5):560-2. PubMed ID: 16215949
    [Abstract] [Full Text] [Related]

  • 45. Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-.
    Vorsanova SG, Yurov YB, Brusquant D, Carles E, Roizes G.
    Tsitol Genet; 2002 Oct; 36(1):46-9. PubMed ID: 12012596
    [Abstract] [Full Text] [Related]

  • 46.
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  • 47. FISH analysis of Y chromosome long arm deletions in subfertile men considering ICSI. A report of two cases.
    Gole LA, Ng SC.
    J Reprod Med; 2002 Jun; 47(6):515-8. PubMed ID: 12092025
    [Abstract] [Full Text] [Related]

  • 48. PCR detection of structurally abnormal Y chromosomes.
    Nagafuchi S, Seki S, Nakahori Y, Tamura T, Numabe H, Nakagome Y.
    Jpn J Hum Genet; 1992 Sep; 37(3):187-93. PubMed ID: 1472700
    [Abstract] [Full Text] [Related]

  • 49. Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q-.
    Mallo M, Arenillas L, Espinet B, Salido M, Hernández JM, Lumbreras E, del Rey M, Arranz E, Ramiro S, Font P, González O, Renedo M, Cervera J, Such E, Sanz GF, Luño E, Sanzo C, González M, Calasanz MJ, Mayans J, García-Ballesteros C, Amigo V, Collado R, Oliver I, Carbonell F, Bureo E, Insunza A, Yañez L, Muruzabal MJ, Gómez-Beltrán E, Andreu R, León P, Gómez V, Sanz A, Casasola N, Moreno E, Alegre A, Martín ML, Pedro C, Serrano S, Florensa L, Solé F.
    Haematologica; 2008 Jul; 93(7):1001-8. PubMed ID: 18591625
    [Abstract] [Full Text] [Related]

  • 50. [Satellited Y chromosome (Yqs) and nucleolar organizer occurring de novo].
    Turleau C, Chavin-Colin F, Seger J, Sorin M, Salet D, de Grouchy J.
    Ann Genet; 1978 Dec; 21(4):239-42. PubMed ID: 314264
    [Abstract] [Full Text] [Related]

  • 51. Molecular and cytogenetic characterization of extra-structurally abnormal chromosomes (ESACs) found prenatally: outcome and follow-up.
    Marchina E, Piovani G, Vezzola L, Bellotti D, Cerri V, Groli C, Barlati S.
    Prenat Diagn; 2003 Dec 15; 23(12):959-63. PubMed ID: 14663830
    [Abstract] [Full Text] [Related]

  • 52. Molecular cytogenetic characterization of three familial cases of satellited Y chromosomes.
    Wilkinson TA, Crolla JA.
    Hum Genet; 1993 May 15; 91(4):389-91. PubMed ID: 8500794
    [Abstract] [Full Text] [Related]

  • 53. Development and targeted application of a rapid QF-PCR test for sex chromosome imbalance.
    Donaghue C, Roberts A, Mann K, Ogilvie CM.
    Prenat Diagn; 2003 Mar 15; 23(3):201-10. PubMed ID: 12627420
    [Abstract] [Full Text] [Related]

  • 54. [Detection of Y chromosome microdeletions in semen of patients with azoospermia: study of 241 cases].
    Li HG, Ding XF, Wang C, Zhao JX, Zuo MD, Xiong CL.
    Zhonghua Yi Xue Za Zhi; 2008 Jun 24; 88(24):1662-5. PubMed ID: 19024532
    [Abstract] [Full Text] [Related]

  • 55. Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16.
    Hengstschläger M, Bettelheim D, Drahonsky R, Deutinger J, Bernaschek G.
    Prenat Diagn; 2001 Jun 24; 21(6):477-80. PubMed ID: 11438953
    [Abstract] [Full Text] [Related]

  • 56. Strategies for the isolation and detection of fetal cells in transcervical samples.
    Bussani C, Cioni R, Scarselli B, Barciulli F, Bucciantini S, Simi P, Fogli A, Scarselli G.
    Prenat Diagn; 2002 Dec 24; 22(12):1098-101. PubMed ID: 12454965
    [Abstract] [Full Text] [Related]

  • 57. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb 24; 26(2):138-46. PubMed ID: 16470734
    [Abstract] [Full Text] [Related]

  • 58. Y chromosome microdeletions: are they implicated in teratozoospermia?
    Hellani A, Al-Hassan S, Al-Duraihim A, Coskun S.
    Hum Reprod; 2005 Dec 24; 20(12):3505-9. PubMed ID: 16123092
    [Abstract] [Full Text] [Related]

  • 59. [Detection of Y chromosome microdeletions in patients with severe oligozoospermia and azoospermia].
    Song NH, Wu HF, Zhang W, Hua LX, Zhou ZM, Feng NH, Zhang J, Qiao D, Zhang JX.
    Zhonghua Yi Xue Za Zhi; 2006 May 30; 86(20):1376-80. PubMed ID: 16796918
    [Abstract] [Full Text] [Related]

  • 60. A case of an intersex horse with 63,X/64,XX/65,XX,del(Y)(q?) karyotype.
    Bugno M, Zabek T, Golonka P, Pieńkowska-Schelling A, Schelling C, Słota E.
    Cytogenet Genome Res; 2008 May 30; 120(1-2):123-6. PubMed ID: 18467835
    [Abstract] [Full Text] [Related]

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