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Journal Abstract Search

216 related items for PubMed ID: 308344

  • 1. A case of partial 9p monosomy with some unusual clinical features.
    Rutten FJ, Hustinx TW, Dunk-Tillemans AA, Scheres JM, Tjon YS.
    Ann Genet; 1978 Mar; 21(1):51-5. PubMed ID: 308344
    [Abstract] [Full Text] [Related]

  • 2. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
    van Balkom ID, Hagendoorn J, De Pater JM, Hennekam RC.
    Genet Couns; 1992 Mar; 3(2):83-9. PubMed ID: 1642815
    [Abstract] [Full Text] [Related]

  • 3. [Rethoré syndrome (9p trisomy) with unusual karyotype: 46,XX,-9, + der 9p, t(9;9)mat].
    Di Cesare D, Paludetto R, Casullo C, Pagano L, Stabile M, Sicolo A, Ventruto V.
    Minerva Pediatr; 1980 Dec 15; 32(23):1349-52. PubMed ID: 7219376
    [No Abstract] [Full Text] [Related]

  • 4. Langer-Giedion syndrome with interstitial 8q-deletion.
    Zabel BU, Baumann WA.
    Am J Med Genet; 1982 Mar 15; 11(3):353-8. PubMed ID: 7081298
    [Abstract] [Full Text] [Related]

  • 5. [Clinical picture of partial monosomy of chromosome 11 q].
    Dörr U.
    Monatsschr Kinderheilkd; 1986 Nov 15; 134(11):808-11. PubMed ID: 3807920
    [Abstract] [Full Text] [Related]

  • 6. Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.
    Okten G, Sezer O, Günes S, Küçüködük S, Oğur G.
    Genet Couns; 2009 Nov 15; 20(4):341-7. PubMed ID: 20162869
    [Abstract] [Full Text] [Related]

  • 7. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
    Serra A, Bova R, Bellanova G, Chindemi A, Zappata S, Brahe C.
    Am J Med Genet; 1997 Aug 08; 71(2):139-43. PubMed ID: 9217211
    [Abstract] [Full Text] [Related]

  • 8. De novo partial monosomy 21 with unusual karyotype.
    Al-Awadi SA, Naguib KK, Teebi AS, Sundareshan TS.
    Jinrui Idengaku Zasshi; 1986 Mar 08; 31(1):45-8. PubMed ID: 3735757
    [No Abstract] [Full Text] [Related]

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  • 10. [Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father].
    Turleau C, De Grouchy J, Roubin M, Chavin-Colin F, Cachin O.
    Ann Genet; 1975 Jun 08; 18(2):125-9. PubMed ID: 1081365
    [Abstract] [Full Text] [Related]

  • 11. [9p monosomy. About a new case. Clinical and cytogenetic study (author's transl)].
    Lajarrige C, Bouquier JJ, Ronayette D, Tchertoff C, Faugeras C, Barthe D, Laleu J.
    Ann Pediatr (Paris); 1979 Nov 08; 26(9):631-6. PubMed ID: 555637
    [No Abstract] [Full Text] [Related]

  • 12. The 9p- syndrome.
    Alfi OS, Donnell GN, Allderdice PW, Derencsenyi A.
    Ann Genet; 1976 Mar 08; 19(1):11-6. PubMed ID: 1084115
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  • 15. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
    Destiné ML, Punnett HH, Thovichit S, DiGeorge AM, Weiss L.
    Ann Genet; 1967 Jun 08; 10(2):65-9. PubMed ID: 5298975
    [No Abstract] [Full Text] [Related]

  • 16. 9p duplication confirmed by gene dosage effect: report of two patients.
    Zadeh TM, Funderburk SJ, Carrel R, Dumars KW.
    Ann Genet; 1981 Jun 08; 24(4):242-4. PubMed ID: 6977307
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  • 18. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
    Cousineau AJ, Higgins JV, Scott-Emuakpor AB, Mody G.
    Am J Med Genet; 1983 Jan 08; 14(1):29-35. PubMed ID: 6829609
    [Abstract] [Full Text] [Related]

  • 19. [Proximal monosomy 13].
    Geormăneanu M, Geormăneanu C.
    Ann Genet; 1990 Jan 08; 33(3):176-8. PubMed ID: 2288464
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