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Journal Abstract Search

105 related items for PubMed ID: 1867291

  • 1. Familial translocation 5;14 resulting in an unbalanced offspring.
    Park JP, Edwards MJ, Moeschler JB, Marin-Padilla JM, Berg SZ, Wurster-Hill DH.
    Am J Med Genet; 1991 Jun 01; 39(3):362-6. PubMed ID: 1867291
    [Abstract] [Full Text] [Related]

  • 2. A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six cases.
    Bofinger MK, Opitz JM, Soukup SW, Ekblom LS, Phillips S, Daniel A, Greene EW.
    Am J Med Genet; 1991 Jan 01; 38(1):1-8. PubMed ID: 2012119
    [Abstract] [Full Text] [Related]

  • 3. Chromosome 6/15 translocation with multiple congenital anomalies.
    Ming PM, Goodner DM, Park TS.
    Obstet Gynecol; 1977 Feb 01; 49(2):251-3. PubMed ID: 834413
    [Abstract] [Full Text] [Related]

  • 4. Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2.
    Pivnick EK, Wilroy RS, Summitt JB, Tucker B, Herrod HG, Tharapel AT.
    Am J Med Genet; 1990 Sep 01; 37(1):92-6. PubMed ID: 2240050
    [Abstract] [Full Text] [Related]

  • 5. Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family.
    de Pina Neto JM, Ferrari I.
    Am J Med Genet; 1980 Sep 01; 5(1):25-33. PubMed ID: 7395898
    [Abstract] [Full Text] [Related]

  • 6. Familial t(4;13) with abnormal offspring in three generations.
    Najafzadeh TM, Littman VA, Dumars KW.
    Am J Med Genet; 1983 Sep 01; 16(1):15-22. PubMed ID: 6638065
    [Abstract] [Full Text] [Related]

  • 7. Familial translocation 2;17 with partial trisomy 2q32 leads to 2qter.
    Giliberti P, Celona A, Della Pietra M, De Masi RV, Fioretti G, Pagano L, Renda S, Vetrella A, Ventruto V.
    Ann Genet; 1980 Sep 01; 23(4):249-50. PubMed ID: 6971607
    [Abstract] [Full Text] [Related]

  • 8. Supernumerary derivative (22) syndrome resulting from a maternal balanced translocation.
    Afroze B, Ngu LH, Roziana A, Aminah M, Noor Shahizan A.
    Singapore Med J; 2008 Dec 01; 49(12):e372-4. PubMed ID: 19122939
    [Abstract] [Full Text] [Related]

  • 9. Complex chromosome rearrangements and congenital anomalies.
    Kousseff BG, Nichols P, Essig YP, Miller K, Weiss A, Tedesco TA.
    Am J Med Genet; 1987 Apr 01; 26(4):771-82. PubMed ID: 3591822
    [Abstract] [Full Text] [Related]

  • 10. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
    Shaffer LG, Spikes AS, Macha M, Dunn R.
    J Reprod Med; 1996 May 01; 41(5):367-71. PubMed ID: 8725766
    [Abstract] [Full Text] [Related]

  • 11. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
    Batista DA, Pai GS, Stetten G.
    Am J Med Genet; 1994 Nov 15; 53(3):255-63. PubMed ID: 7856662
    [Abstract] [Full Text] [Related]

  • 12. Familial, balanced insertional translocation of chromosome 7 leading to offspring with deletion and duplication of the inserted segment, 7p15 leads to 7p21.
    Miller M, Kaufman G, Reed G, Bilenker R, Schinzel A.
    Am J Med Genet; 1979 Nov 15; 4(4):323-32. PubMed ID: 539602
    [Abstract] [Full Text] [Related]

  • 13. [A new case of trisomy 5p].
    Antonenko VG, Levina LIa, Chudnova VI.
    Genetika; 1985 Dec 15; 21(12):2066-70. PubMed ID: 4085794
    [Abstract] [Full Text] [Related]

  • 14. Unbalanced translocation in a mother and her son in one of two 5;10 translocation families.
    Barber JC, Temple IK, Campbell PL, Collinson MN, Campbell CM, Renshaw RM, Dennis NR.
    Am J Med Genet; 1996 Mar 01; 62(1):84-90. PubMed ID: 8779332
    [Abstract] [Full Text] [Related]

  • 15. [Trisomy of the distal 15q region due to familial balanced translocation t(15;16)(q24;p13) and unusual mosaicism in the mother of the proband].
    Nazarenko SA, Nazarenko LP, Baranova VA.
    Tsitol Genet; 1987 Mar 01; 21(6):434-7. PubMed ID: 3445362
    [Abstract] [Full Text] [Related]

  • 16. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
    Karmous-Benailly H, Giuliano F, Massol C, Bloch C, De Ricaud D, Lambert JC, Perelman S.
    Eur J Med Genet; 2006 Mar 01; 49(5):431-8. PubMed ID: 16497571
    [Abstract] [Full Text] [Related]

  • 17. 8q22-->qter duplication in a child with multiple congenital malformations: case report.
    Sasiadek M, Stembalska A, Schlade K, Zych M.
    Med Sci Monit; 2000 Mar 01; 6(1):141-4. PubMed ID: 11208302
    [Abstract] [Full Text] [Related]

  • 18. Duplication 7p in a family with t(7;11): association with anomalies of the anterior cranial base.
    Odell JM, Siebert JR, Bradley C, Salk D.
    Am J Med Genet; 1987 Jul 01; 27(3):687-92. PubMed ID: 3631140
    [Abstract] [Full Text] [Related]

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  • 20. Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.
    Zackai EH, Emanuel BS.
    Am J Med Genet; 1980 Jul 01; 7(4):507-21. PubMed ID: 7211960
    [Abstract] [Full Text] [Related]

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