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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

418 related items for PubMed ID: 124130

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Autosomal syndromes.
    Summitt RL.
    Pediatr Ann; 1978 Jun; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
    [No Abstract] [Full Text] [Related]

  • 3. Trisomy 22 in a liveborn infant with multiple congenital anomalies.
    McPherson E, Stetka DG.
    Am J Med Genet; 1990 May; 36(1):11-4. PubMed ID: 2333899
    [Abstract] [Full Text] [Related]

  • 4.
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  • 5. [Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)].
    Laurent C, Bovier-Lapierre M, Dutrillaux B.
    Humangenetik; 1973 May; 18(4):321-7. PubMed ID: 4200006
    [No Abstract] [Full Text] [Related]

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  • 7. Three non-mongoloid patients of similar phenotype with an extra G-like chromosome.
    Gustavson KH, Hitrec V, Santesson B.
    Clin Genet; 1972 May; 3(2):135-46. PubMed ID: 5054315
    [No Abstract] [Full Text] [Related]

  • 8. Trisomy 18.
    James AE, Belcourt CL, Atkins L, Janower ML.
    Radiology; 1969 Jan; 92(1):37-43. PubMed ID: 4236175
    [No Abstract] [Full Text] [Related]

  • 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. Autosomal chromosome aberrations in ophthalmology.
    François J.
    J Neurol Sci; 1967 Mar; 4(3):511-58. PubMed ID: 4228074
    [No Abstract] [Full Text] [Related]

  • 11. Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).
    Cantu JM, Salamanca F, Buentello L, Carnevale A, Armendares S.
    Ann Genet; 1975 Mar; 18(1):5-11. PubMed ID: 1080038
    [Abstract] [Full Text] [Related]

  • 12. Brother and sister with trisomy 10p: a new syndrome.
    Schleiermacher E, Schliebitz U, Steffens C.
    Humangenetik; 1974 Mar; 23(3):163-72. PubMed ID: 4844639
    [No Abstract] [Full Text] [Related]

  • 13. [Eye anomalies in chromosomal aberrations].
    Lur'e IV, Gushchina GS.
    Oftalmol Zh; 1971 Mar; 26(4):299-306. PubMed ID: 4256612
    [No Abstract] [Full Text] [Related]

  • 14. Autosomal chromosome aberrations in ophthalmology.
    Francois J.
    Int Ophthalmol Clin; 1968 Mar; 8(4):839-910. PubMed ID: 4244691
    [No Abstract] [Full Text] [Related]

  • 15.
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  • 16. Trisomy 13-15.
    James AE, Belcourt CL, Atkins L, Janower ML.
    Radiology; 1969 Jan; 92(1):44-9. PubMed ID: 4302761
    [No Abstract] [Full Text] [Related]

  • 17. Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
    Sanchez O, Yunis JJ, Escobar JI.
    Humangenetik; 1974 Apr 24; 22(1):59-65. PubMed ID: 4134840
    [No Abstract] [Full Text] [Related]

  • 18. Reciprocal translocation versus centric fusion between two No. 13 chromosomes. A case of 46,XX,-13,+t(13;13)(p12;q13) and a case of 46,XY,-13,+t(13;13)(p12;p12).
    Hsu LY, Kim HJ, Sujansky E, Kousseff B, Hirschhorn K.
    Cytogenet Cell Genet; 1973 Apr 24; 12(4):235-44. PubMed ID: 4752865
    [No Abstract] [Full Text] [Related]

  • 19.
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  • 20. Human chromosome abnormalities as related to physical and mental dysfunction.
    Heller JH.
    J Hered; 1969 Apr 24; 60(5):239-48. PubMed ID: 4244249
    [No Abstract] [Full Text] [Related]

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