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Journal Abstract Search

145 related items for PubMed ID: 589852

  • 1.
    ; . PubMed ID:
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  • 2. Partial monosomy or trisomy resulting from crossing over within a rearranged chromosome 1.
    Garver KL, Ciocco AM, Turack NA.
    Clin Genet; 1976 Dec; 10(6):319-24. PubMed ID: 991441
    [Abstract] [Full Text] [Related]

  • 3. New chromosomal syndromes.
    Lewandowski RC, Yunis JJ.
    Am J Dis Child; 1975 Apr; 129(4):515-29. PubMed ID: 124130
    [No Abstract] [Full Text] [Related]

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  • 5. Identical multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to del(2)(q32) in two sisters with intrachromosomal insertional translocation in their father.
    Pai GS, Rogers JF, Sommer A.
    Am J Med Genet; 1983 Jan; 14(1):189-95. PubMed ID: 6829607
    [Abstract] [Full Text] [Related]

  • 6. Familial Duplication/Deletion of 1q42.13q43 as Meiotic Consequence of an Intrachromosomal Insertion in Chromosome 1.
    Silipigni R, Monfrini E, Baccarin M, Giangiobbe S, Lalatta F, Guerneri S, Bedeschi MF.
    Cytogenet Genome Res; 2017 Jan; 153(2):73-80. PubMed ID: 29258113
    [Abstract] [Full Text] [Related]

  • 7. Familial partial trisomy 5p resulting from segregation of an insertional translocation.
    Gustavson KH, Lundberg PO, Nicol P.
    Clin Genet; 1988 Jun; 33(6):404-9. PubMed ID: 3168312
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  • 9. Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.
    Lindenbaum RH, Bobrow M.
    J Med Genet; 1975 Mar; 12(1):29-43. PubMed ID: 123589
    [Abstract] [Full Text] [Related]

  • 10. A familial "balanced" 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings.
    Wagstaff J, Hemann M.
    Am J Hum Genet; 1995 Jan; 56(1):302-9. PubMed ID: 7825591
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  • 11. Partial trisomy 8q. Two case reports with maternal translocation and inverted insertion: phenotype analyses and reflections on the risk.
    Stengel-Rutkowski S, Lohse K, Herzog C, Apacik C, Couturier J, Albert A, Belohradsky B.
    Clin Genet; 1992 Oct; 42(4):178-85. PubMed ID: 1424241
    [Abstract] [Full Text] [Related]

  • 12. Segregation of an insertional chromosome rearrangement in 3 generations.
    Toomey KE, Mohandas T, Sparkes RS, Kaback MM, Rimoin DL.
    J Med Genet; 1978 Oct; 15(5):382-7. PubMed ID: 739529
    [Abstract] [Full Text] [Related]

  • 13. Reproductive outcomes of paracentric inversion carriers: report of a liveborn dicentric recombinant and literature review.
    Mules EH, Stamberg J.
    Hum Genet; 1984 Oct; 67(2):126-31. PubMed ID: 6745933
    [Abstract] [Full Text] [Related]

  • 14. 'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations.
    Brimblecombe FS, Lewis FJ, Vowles M.
    J Med Genet; 1977 Aug; 14(4):271-4. PubMed ID: 926139
    [Abstract] [Full Text] [Related]

  • 15. A child with partial trisomy of chromosome 17 and partial monosomy of chromosome 3: 46,XY,der(3),t(3;17)(p25;q23).
    Shawe DJ, Fear C, Appleyard WJ.
    J Med Genet; 1983 Oct; 20(5):383-5. PubMed ID: 6196484
    [Abstract] [Full Text] [Related]

  • 16. The 2p partial trisomy syndrome. Duplication of region 2p23 leads to 2pter in two members of a t(2;7) translocation kindred.
    Francke U, Jones KL.
    Am J Dis Child; 1976 Nov; 130(11):1244-9. PubMed ID: 984008
    [Abstract] [Full Text] [Related]

  • 17. Partial trisomy for the short arm of chromosome 2 due to familial balance translocation.
    Sekhon GS, Taysi K, Rath R.
    Hum Genet; 1978 Oct 19; 44(1):99-103. PubMed ID: 711241
    [Abstract] [Full Text] [Related]

  • 18. Familial partial trisomy of the long arm of chromosome 10 (q24-26).
    Moreno-Fuenmayor H, Zackai EH, Mellman WJ, Aronson M.
    Pediatrics; 1975 Nov 19; 56(5):756-61. PubMed ID: 1196732
    [Abstract] [Full Text] [Related]

  • 19. Reproductive possibilities for balanced translocation (14) carriers in families with partial trisomy of proximal 14q.
    Valkova G, Stefanova M.
    J Med Genet; 1993 Jan 19; 30(1):73-5. PubMed ID: 8423613
    [Abstract] [Full Text] [Related]

  • 20. Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7.
    Winsor EJ, Palmer CG, Ellis PM, Hunter JL, Ferguson-Smith MA.
    Cytogenet Cell Genet; 1978 Jan 19; 20(1-6):169-84. PubMed ID: 648176
    [Abstract] [Full Text] [Related]

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