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Journal Abstract Search

252 related items for PubMed ID: 30204977

  • 21. Genitourinary anomalies of pediatric FG syndrome.
    Smith JF, Wayment RO, Cartwright PC, Snow BW, Opitz JM.
    J Urol; 2007 Aug; 178(2):656-9. PubMed ID: 17574621
    [Abstract] [Full Text] [Related]

  • 22. Pigmentary mosaicism with trisomy 7.
    Park MY, Jin H, You HS, Shim WH, Kim GW, Kim HS, Kim BS, Kim MB, Ko HC.
    J Dermatol; 2018 Feb; 45(2):e47-e48. PubMed ID: 29047159
    [No Abstract] [Full Text] [Related]

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  • 24. Mosaic supernumerary r(8) syndrome.
    Yilmaz S, Tarkan-Argüden Y, Kuru D, Deviren A, Karaman B, Yüksel A, Hacihanefioğlu S.
    Genet Couns; 2005 Feb; 16(2):187-90. PubMed ID: 16080301
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  • 29. Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes.
    Liehr T, Klein E, Mrasek K, Kosyakova N, Guilherme RS, Aust N, Venner C, Weise A, Hamid AB.
    Cytogenet Genome Res; 2013 Feb; 139(3):158-63. PubMed ID: 23295254
    [Abstract] [Full Text] [Related]

  • 30. A CASE OF CONFINED PLACENTAL MOSAICISM WITH TRISOMY 15 ASSOCIATED WITH TURNER SYNDROME.
    Ekici C, Sahin Y, Yaykasli KO, Melekoglu R, Sahin N, Yuksel S.
    Genet Couns; 2016 Feb; 27(4):485-488. PubMed ID: 30226967
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  • 31. Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome.
    Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Chen WL, Wang W.
    Taiwan J Obstet Gynecol; 2017 Apr; 56(2):268-269. PubMed ID: 28420524
    [No Abstract] [Full Text] [Related]

  • 32. Partial trisomy 8 mosaicism not detected by cultured amniotic-fluid cells.
    Tsai MC, Cheng HY, Su MT, Chen M, Kuo PL.
    Taiwan J Obstet Gynecol; 2014 Dec; 53(4):598-601. PubMed ID: 25510708
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  • 33. Maternal uniparental disomy 14 dissection of the phenotype with respect to rare autosomal recessively inherited traits, trisomy mosaicism, and genomic imprinting.
    Kotzot D.
    Ann Genet; 2004 Dec; 47(3):251-60. PubMed ID: 15337470
    [Abstract] [Full Text] [Related]

  • 34. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
    Mutesa L, Hellin AC, Jamar M, Pierquin G, Bours V, Verloes A.
    Genet Couns; 2007 Dec; 18(2):201-7. PubMed ID: 17710872
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  • 35. Similar but different: identical pathology with differing outcome in 'Not-so-identical' twins.
    Butler GH, Flood K, Doyle E, Geary MP, Betts DR, Foran A, O'Marcaigh A, Cotter M.
    Br J Haematol; 2017 Jul; 178(1):152-153. PubMed ID: 27102370
    [No Abstract] [Full Text] [Related]

  • 36. Disappearance of the trisomy 15 cell line at long-term follow-up in mosaic trisomy 15 at amniocentesis.
    Chen CP.
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):373. PubMed ID: 33678347
    [No Abstract] [Full Text] [Related]

  • 37. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
    Brambila-Tapia AJ, Neira VA, Vásquez-Velásquez AI, Jimenez-Arredondo RE, Chávez-González EL, Picos-Cárdenas VJ, Fletes-Rayas AL, Figuera LE.
    Genet Couns; 2014 Mar; 25(3):289-97. PubMed ID: 25365851
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  • 38. Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.
    Schinzel A, Kotzot D, Brecevic L, Robinson WP, Dutly F, Dauwerse H, Binkert F, Baumer A, Ausserer B.
    Eur J Hum Genet; 1997 Mar; 5(5):308-14. PubMed ID: 9412788
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  • 39. Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability.
    Naoufal R, Legendre M, Couet D, Gilbert-Dussardier B, Kitzis A, Bilan F, Harbuz R.
    Eur J Med Genet; 2016 Sep; 59(9):483-7. PubMed ID: 27452446
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  • 40. A severely short-statured girl with 47,XX, + 14/46,XX,upd(14)mat, mosaicism.
    Ushijima K, Yatsuga S, Matsumoto T, Nakamura A, Fukami M, Kagami M.
    J Hum Genet; 2018 Mar; 63(3):377-381. PubMed ID: 29311684
    [Abstract] [Full Text] [Related]

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