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Journal Abstract Search

209 related items for PubMed ID: 6604493

  • 1. Trisomy 20p due to a paternal reciprocal translocation.
    Funderburk SJ, Sparkes RS, Sparkes MC.
    Ann Genet; 1983; 26(2):94-7. PubMed ID: 6604493
    [Abstract] [Full Text] [Related]

  • 2. "De Novo" trisomy 20p with macroorchidism in a prepuberal boy.
    Balestrazzi P, Virdis R, Frassi C, Negri V, Rigoli E, Bernasconi S.
    Ann Genet; 1984; 27(1):58-9. PubMed ID: 6609676
    [Abstract] [Full Text] [Related]

  • 3. Trisomy 20p: case report and genetic review.
    Lurie IW, Rumyantseva NV, Zaletajev DV, Gurevich DB, Korotkova IA.
    J Genet Hum; 1985 Jan; 33(1):67-75. PubMed ID: 3981145
    [Abstract] [Full Text] [Related]

  • 4. Familial trisomy 20p five cases and two carriers in three generations a review.
    Centerwall W, Francke U.
    Ann Genet; 1977 Jun; 20(2):77-83. PubMed ID: 302689
    [Abstract] [Full Text] [Related]

  • 5. [Translocation trisomy 4q in 2 siblings as a sequela of paternal balanced reciprocal translocation: t(1;4)(q44;q31)].
    Bode H, Bühler EM, Wyler F, Hadzilselimovic F.
    Monatsschr Kinderheilkd; 1990 Nov; 138(11):763-6. PubMed ID: 2290435
    [Abstract] [Full Text] [Related]

  • 6. Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features.
    Mégarbané A, Souraty N, Theophile D, Vekemans M, Samaras L, Ghorayeb Z.
    Ann Genet; 1997 Nov; 40(1):55-9. PubMed ID: 9150851
    [Abstract] [Full Text] [Related]

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

  • 8. Triplication of chromosome arm 20p due to inherited translocation and secondary nondisjunction.
    Marcus ES, Fuller B, Riccardi VM.
    Am J Med Genet; 1979 Dec; 4(1):47-50. PubMed ID: 495652
    [Abstract] [Full Text] [Related]

  • 9. [Case of partial trisomy 4p+ in a child as a result of a balanced translocation in the father].
    Patiutko RS, Kulieva LM, Egolina NA.
    Genetika; 1978 Sep; 14(9):1653-7. PubMed ID: 720831
    [Abstract] [Full Text] [Related]

  • 10. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
    de Ravel T, Aerssens P, Vermeesch JR, Fryns JP.
    Eur J Med Genet; 2005 Sep; 48(3):355-9. PubMed ID: 16179232
    [Abstract] [Full Text] [Related]

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  • 12. Report of a trisomy 8p infant with carrier father.
    Funderburk SJ, Barrett CT, Klisak I.
    Ann Genet; 1978 Dec; 21(4):219-22. PubMed ID: 314258
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  • 14. [11q distal trisomy due to a familial 11;18 translocation].
    Menéndez I, Rivera H, Morales E, Juan J, Jiménez M.
    Bol Med Hosp Infant Mex; 1990 Nov; 47(11):792-4. PubMed ID: 2285470
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  • 16. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
    Ausems MG, Van Spijker HG, Dijkhuis HJ, Swanenburg De Veye HF, Bijlsma JB.
    Genet Couns; 1996 Nov; 7(1):61-5. PubMed ID: 8652090
    [Abstract] [Full Text] [Related]

  • 17. [Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities].
    Xiao B, Zhang JM, Ji X, Jiang WT, Hu J, Tao J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):247-50. PubMed ID: 21644216
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  • 19. Malformation syndrome of duplication 12q24.1 leads to qter.
    Melnyk AR, Weiss L, Van Dyke DL, Jarvi P.
    Am J Med Genet; 1981 Jun; 10(4):357-65. PubMed ID: 7332029
    [Abstract] [Full Text] [Related]

  • 20. 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]

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