These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

284 related items for PubMed ID: 6513939

  • 1. [Phenotype of trisomy 9].
    Pfeiffer RA, Müller R.
    Monatsschr Kinderheilkd; 1984 Oct; 132(10):797-800. PubMed ID: 6513939
    [Abstract] [Full Text] [Related]

  • 2. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.
    Shapiro SD, Hansen KL, Littlefield CA.
    Am J Med Genet; 1985 Feb; 20(2):271-6. PubMed ID: 3976720
    [Abstract] [Full Text] [Related]

  • 3. [Partial trisomy C by t(Cq-; Dp+) translocation with a C(p- q+) remnant].
    De Grouchy J, Thieffry S, Aicardi J, Chevrie JJ, Zucker G.
    Arch Fr Pediatr; 1967 Oct; 24(8):859-68. PubMed ID: 5584189
    [No Abstract] [Full Text] [Related]

  • 4. [Chromosomal studies in craniofacial abnormalities].
    Ahrens K.
    HNO; 1967 Apr; 15(4):106-9. PubMed ID: 5592377
    [No Abstract] [Full Text] [Related]

  • 5. Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).
    Cantu JM, Salamanca F, Buentello L, Carnevale A, Armendares S.
    Ann Genet; 1975 Mar; 18(1):5-11. PubMed ID: 1080038
    [Abstract] [Full Text] [Related]

  • 6. [Tetrasomy 9p].
    Foerster W, Koch M, Hansen S.
    Monatsschr Kinderheilkd; 1985 Sep; 133(9):694-7. PubMed ID: 2865673
    [Abstract] [Full Text] [Related]

  • 7. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q?
    Riegel M, Schinzel A.
    Am J Med Genet; 2002 Jul 22; 111(1):76-80. PubMed ID: 12124740
    [Abstract] [Full Text] [Related]

  • 8. 12q interstitial deletion with bilateral cleft lip and palate: case report and literature review.
    Yamanishi T, Nishio J, Miya S, Okamoto N, Takahashi A, Toribe Y, Mukai T, Kobayashi C.
    Cleft Palate Craniofac J; 2008 May 22; 45(3):325-8. PubMed ID: 18452363
    [Abstract] [Full Text] [Related]

  • 9. The phenotypic and cytogenetic spectrum of partial trisomy 9.
    Wilson GN, Raj A, Baker D.
    Am J Med Genet; 1985 Feb 22; 20(2):277-82. PubMed ID: 3976721
    [Abstract] [Full Text] [Related]

  • 10. Familial 10p trisomy resulting from a maternal pericentric inversion.
    Kozma C, Meck JM.
    Am J Med Genet; 1994 Feb 01; 49(3):281-7. PubMed ID: 8209887
    [Abstract] [Full Text] [Related]

  • 11. Monosomy and trisomy of 15q24-qter with cleft lip and palate.
    Abe A, Hatano Y, Kurita K, Nakano M, Shimizu M, Yokoi T, Sugiyama N.
    Int J Oral Maxillofac Surg; 2008 May 01; 37(5):487-90. PubMed ID: 18262763
    [Abstract] [Full Text] [Related]

  • 12. "Pure" partial trisomy 3p due to the malsegregation of a balanced maternal translocation t (X;3) (p22.3;p21).
    de Almeida JC, Reis DF, Llerena JC, Pereira ET.
    Ann Genet; 1989 May 01; 32(3):181-3. PubMed ID: 2817779
    [Abstract] [Full Text] [Related]

  • 13. Report of a trisomy 8p infant with carrier father.
    Funderburk SJ, Barrett CT, Klisak I.
    Ann Genet; 1978 Dec 01; 21(4):219-22. PubMed ID: 314258
    [Abstract] [Full Text] [Related]

  • 14. Cleft palate and multiple anomalies in one of two siblings with partial 13 trisomy.
    Kaye CI, Booth CW, Meeker D, Nadler HL.
    Cleft Palate J; 1977 Jul 01; 14(3):244-8. PubMed ID: 267527
    [Abstract] [Full Text] [Related]

  • 15. Trisomy 22 confirmed by fluorescent in situ hybridization.
    Stratton RF, DuPont BR, Mattern VL, Young RS, McCourt JW, Moore CM.
    Am J Med Genet; 1993 Apr 01; 46(1):109-12. PubMed ID: 8494030
    [Abstract] [Full Text] [Related]

  • 16. Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature.
    Plotner PL, Smith JL, Northrup H.
    Am J Med Genet; 2002 Jul 22; 111(1):71-5. PubMed ID: 12124739
    [Abstract] [Full Text] [Related]

  • 17. Dermatoglyphics in children suffering from congenital defects, with and without chromosomal aberrations.
    Usoev SS.
    Sov Genet; 1974 Jul 15; 8(7):929-31. PubMed ID: 4278489
    [No Abstract] [Full Text] [Related]

  • 18. [Fluorescence and Giemsa-banding in a case of Pätau's syndrome].
    Golob E, Schaller A.
    Zentralbl Gynakol; 1974 Oct 11; 96(41):1305-8. PubMed ID: 4142346
    [No Abstract] [Full Text] [Related]

  • 19. Mosaic trisomy 9 syndrome with unusual phenotype.
    Kaminker CP, Daín L, Lamas MA, Sánchez JM.
    Am J Med Genet; 1985 Oct 11; 22(2):237-41. PubMed ID: 3931476
    [Abstract] [Full Text] [Related]

  • 20. Oral-facial-digital (OFD) syndrome with associated features: a new syndrome or genetic heterogeneity and variability?
    Morán-Barroso V, Valdés Flores M, García-Cavazos R, Kofman-Alfaro S, Saavedra-Ontiveros D.
    Clin Dysmorphol; 1998 Jan 11; 7(1):55-7. PubMed ID: 9546832
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.