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586 related items for PubMed ID: 10631922

  • 1. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
    Grammatico P, Majore S, Marrocco G, Poscente M, Mordenti C, Grammatico B, Del Porto G.
    Genet Couns; 1999; 10(4):351-8. PubMed ID: 10631922
    [Abstract] [Full Text] [Related]

  • 2. Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10p.
    Grossi A, Palma A, Zanni G, Novelli A, Loddo S, Cappa M, Fierabracci A.
    Gene; 2013 Feb 25; 515(2):439-43. PubMed ID: 23262341
    [Abstract] [Full Text] [Related]

  • 3. A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.
    Courtens W, Wuyts W, Scheers S, Van Luijk R, Reyniers E, Rooms L, Ceulemans B, Kooy F, Wauters J.
    Eur J Med Genet; 2006 Feb 25; 49(5):402-13. PubMed ID: 16488200
    [Abstract] [Full Text] [Related]

  • 4. 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 Feb 25; 20(4):341-7. PubMed ID: 20162869
    [Abstract] [Full Text] [Related]

  • 5. Combined 10pter-->p11 and 18pter-->q11 trisomy in a 7-year-old child.
    Lapière JC, Verloes A, Herens C, Delfortrie J, Van Maldergem L, Gillerot Y, Koulischer L.
    Genet Couns; 1992 Feb 25; 3(3):155-9. PubMed ID: 1388935
    [Abstract] [Full Text] [Related]

  • 6. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
    van Balkom ID, Hagendoorn J, De Pater JM, Hennekam RC.
    Genet Couns; 1992 Feb 25; 3(2):83-9. PubMed ID: 1642815
    [Abstract] [Full Text] [Related]

  • 7. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.
    Okada M, Usami A, Okajima K, Yamada M, Yamaguchi Y, Umezaki I, Matsuda Y, Ohta H.
    Congenit Anom (Kyoto); 2005 Dec 25; 45(4):161-4. PubMed ID: 16359498
    [Abstract] [Full Text] [Related]

  • 8. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS, Kamel AK, Helmy NA.
    Genet Couns; 2008 Dec 25; 19(2):199-209. PubMed ID: 18618995
    [Abstract] [Full Text] [Related]

  • 9. DiGeorge syndrome and partial monosomy 10p: case report and review.
    Schuffenhauer S, Seidel H, Oechsler H, Belohradsky B, Bernsau U, Murken J, Meitinger T.
    Ann Genet; 1995 Dec 25; 38(3):162-7. PubMed ID: 8540688
    [Abstract] [Full Text] [Related]

  • 10. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
    Gentile M, Buonadonna AL, Cariola F, Fiorente P, Valenzano MC, Guanti G.
    J Med Genet; 1999 Jan 25; 36(1):77-82. PubMed ID: 9950374
    [Abstract] [Full Text] [Related]

  • 11. [Trisomy of the short arm of chromosome 10p; description of a female patient with de novo duplication 10p11.2-15].
    Fechtrup B, Kalhoff H, Diekmann L, Fritz B.
    Klin Padiatr; 2000 Jan 25; 212(1):35-40. PubMed ID: 10719682
    [Abstract] [Full Text] [Related]

  • 12. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B, Hacihanefioglu S, Silahtaroglu A, Yilmaz S, Deviren A, Cenani A.
    Genet Couns; 2000 Jan 25; 11(4):355-61. PubMed ID: 11140413
    [Abstract] [Full Text] [Related]

  • 13. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
    Frankova YE, Holenova H, Braulke I.
    Monatsschr Kinderheilkd; 1991 Dec 25; 139(12):841-3. PubMed ID: 1770961
    [Abstract] [Full Text] [Related]

  • 14. [Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)].
    Obry E, Piussan C, Risbourg B, Dutrillaux B.
    Ann Genet; 1980 Dec 25; 23(4):216-20. PubMed ID: 6971599
    [Abstract] [Full Text] [Related]

  • 15. [Clinical and molecular cytogenetic analysis of a rare case of mosaicism for partial monosomy 3p and partial trisomy 10q in human].
    Karamysheva TV, Matveeva VG, Shorina AP, Rubtsov NB.
    Genetika; 2001 Jun 25; 37(6):811-6. PubMed ID: 11517768
    [Abstract] [Full Text] [Related]

  • 16. [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].
    Vivarelli R, Paolieri M, Anichini C, Scarinci R, Berardi R, Rosaia L, Pucci L.
    Boll Soc Ital Biol Sper; 1992 Apr 25; 68(4):263-9. PubMed ID: 1463601
    [Abstract] [Full Text] [Related]

  • 17. [46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)].
    Turleau C, Rethoré MO, Junien C, Lejeune J, de Grouchy J.
    Ann Genet; 1979 Apr 25; 22(3):178-81. PubMed ID: 316677
    [Abstract] [Full Text] [Related]

  • 18. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
    Hegmann KM, Spikes AS, Orr-Urtreger A, Shaffer LG.
    Am J Med Genet; 1996 Jan 02; 61(1):10-5. PubMed ID: 8741910
    [Abstract] [Full Text] [Related]

  • 19. Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype.
    Krasikov N, Takaesu N, Hassold T, Knops JF, Finley WH, Scarbrough P.
    Am J Med Genet; 1992 Jun 01; 43(3):554-60. PubMed ID: 1605248
    [Abstract] [Full Text] [Related]

  • 20. Partial monosomy 10p syndrome.
    Koenig R, Kessel E, Schoenberger W.
    Ann Genet; 1985 Jun 01; 28(3):173-6. PubMed ID: 3879152
    [Abstract] [Full Text] [Related]

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