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240 related items for PubMed ID: 11438955
21. Male infertility: polymerase chain reaction-based deletion mapping of genes on the human chromosome. Viswambharan N, Suganthi R, Simon AM, Manonayaki S. Singapore Med J; 2007 Dec; 48(12):1140-2. PubMed ID: 18043844 [Abstract] [Full Text] [Related]
22. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype. Beaujard MP, Jouannic JM, Bessières B, Borie C, Martin-Luis I, Fallet-Bianco C, Portnoï MF. Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060 [Abstract] [Full Text] [Related]
23. Prenatal identification of an isochromosome for the short arm of the Y i(Yp), by cytogenetic and molecular analyses. Slim R, Soulié J, Hotmar J, Lecolier B, Bercau G, Bernheim A. Prenat Diagn; 1994 Jan; 14(1):23-8. PubMed ID: 8183834 [Abstract] [Full Text] [Related]
24. Molecular analysis of Y chromosome microdeletions in idiopathic cases of male infertility in Serbia. Ristanovic M, Bunjevacki V, Tulic C, Novakovic I, Nikolic A. Genetika; 2007 Jun; 43(6):850-4. PubMed ID: 17853812 [Abstract] [Full Text] [Related]
25. Evaluation of satellited Y chromosome (Yqs) detected during prenatal diagnosis. Haddad BR, Huang Y, Wyandt H, Milunsky A. Acta Obstet Gynecol Scand; 1997 Mar; 76(3):281-3. PubMed ID: 9093147 [No Abstract] [Full Text] [Related]
26. Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis. Aktas D, Alikasifoglu M, Gonc N, Senocak ME, Tuncbilek E. Eur J Med Genet; 2006 Mar; 49(2):141-9. PubMed ID: 16530711 [Abstract] [Full Text] [Related]
27. [Screening for Y chromosome sequences in patients with Turner syndrome]. Ferrão L, Lopes ML, Limbert C, Marques B, Boieiro F, Silva M, Marques R, Lavinha J, Mota A, Gonçalves J. Acta Med Port; 2002 Mar; 15(2):89-100. PubMed ID: 15524154 [Abstract] [Full Text] [Related]
28. Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3. Christopoulou G, Tzetis M, Konstantinidou AE, Tsezou A, Kanavakis E, Kitsiou-Tzeli S, Velissariou V. Eur J Med Genet; 2012 Jan; 55(1):75-9. PubMed ID: 21914491 [Abstract] [Full Text] [Related]
29. 47,XX + mar karyotype containing genes from the azoospermia factor region. A case report. Causio F, Gentile E, Fischetto R, Archidiacono N, Magro N. J Reprod Med; 2002 Jul; 47(7):575-80. PubMed ID: 12170536 [Abstract] [Full Text] [Related]
30. Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic man. Valetto A, Bertini V, Rapalini E, Baldinotti F, Di Martino D, Simi P. Fertil Steril; 2004 May; 81(5):1388-90. PubMed ID: 15136108 [Abstract] [Full Text] [Related]
31. Origin and structure of a satellited Y chromosome. Martin Lucas MA, Pérez Castillo A, Abrisqueta JA. Ann Genet; 1984 May; 27(3):184-6. PubMed ID: 6334485 [Abstract] [Full Text] [Related]
32. Delineating the association between isodicentric chromosome Y and infertility: a retrospective study. Kalantari H, Asia S, Totonchi M, Vazirinasab H, Mansouri Z, Zarei Moradi S, Haratian K, Gourabi H, Mohseni Meybodi A. Fertil Steril; 2014 Apr; 101(4):1091-6. PubMed ID: 24502892 [Abstract] [Full Text] [Related]
33. Characterisation of a satellited non-fluorescent Y chromosome (Y[nfqs]) by FISH. Verma RS, Gogineni SK, Kleyman SM, Conte RA. J Med Genet; 1997 Oct; 34(10):817-8. PubMed ID: 9350813 [Abstract] [Full Text] [Related]
34. Loss of the Y chromosomal PAR2-region in four familial cases of satellited Y chromosomes (Yqs). Kühl H, Röttger S, Heilbronner H, Enders H, Schempp W. Chromosome Res; 2001 Oct; 9(3):215-22. PubMed ID: 11330396 [Abstract] [Full Text] [Related]
35. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs. Giardino D, Corti C, Ballarati L, Finelli P, Valtorta C, Botta G, Giudici M, Grosso E, Larizza L. Prenat Diagn; 2006 Jun; 26(6):565-70. PubMed ID: 16683274 [Abstract] [Full Text] [Related]
36. A case of prenatal diagnosis of a familial satellited Yq chromosome. Tsita KP, Vallas OS, Velissariou PJ, Lyberatou-Moraitou EK. Clin Genet; 1989 Jan; 35(1):70-4. PubMed ID: 2924432 [Abstract] [Full Text] [Related]
37. Prenatal diagnosis and prenatal imaging of a de novo 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalities. Ghosh A, Higgins L, Larkins SA, Miller C, Ostojic N, Martin WL, Kilby MD. Prenat Diagn; 2008 Nov; 28(11):1068-71. PubMed ID: 18925617 [No Abstract] [Full Text] [Related]
38. Prenatal detection of a de novo Yqh-acrocentric translocation. Ng LK, Kwok YK, Tang LY, Ng PP, Ghosh A, Lau ET, Tang MH. Clin Biochem; 2006 Mar; 39(3):219-23. PubMed ID: 16515778 [Abstract] [Full Text] [Related]
39. Characterization of a de novo balanced 1;Y translocation in a phenotypically normal twin male infant. Hatzissevastou-Loukidou H, Kalemi TG, Lambropoulos AF, Nikita M, Sotiridou E, Tarlatzis BC, Kotsis A. Fertil Steril; 2006 Apr; 85(4):1059.e5-7. PubMed ID: 16580398 [Abstract] [Full Text] [Related]
40. Mosaic ring Y chromosome in two normal healthy men with azoospermia. Bertini V, Canale D, Bicocchi MP, Simi P, Valetto A. Fertil Steril; 2005 Dec; 84(6):1744. PubMed ID: 16359976 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]