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Journal Abstract Search

742 related items for PubMed ID: 4261167

  • 1. Structural variation in human nitotic chromosomes.
    Leisti J.
    Ann Acad Sci Fenn Biol; 1971; 179():1-69. PubMed ID: 4261167
    [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. Autosomal chromosome aberrations in ophthalmology.
    Francois J.
    Int Ophthalmol Clin; 1968 Jun; 8(4):839-910. PubMed ID: 4244691
    [No Abstract] [Full Text] [Related]

  • 4. [The "Copenhagen chromosome" (syndrome of the small metacentric extra-chromosome)].
    Haberlandt W.
    Arztl Forsch; 1971 Jul 10; 25(7):218-23. PubMed ID: 5109598
    [No Abstract] [Full Text] [Related]

  • 5. Human chromosome identification and the pattern of DNA replication in fibroblasts from an XXY male. A quantitative autoradiographic study of early and late synthesis.
    Ockey CH.
    Cytogenetics; 1969 Jul 10; 8(4):272-95. PubMed ID: 4245462
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA, Mikel'saar AV, Mikel'saar RV.
    Sov Genet; 1974 Jun 01; 8(5):651-7. PubMed ID: 4413436
    [No Abstract] [Full Text] [Related]

  • 8. Clinical, cytogeneti and autoradiographic studies in 0 cases with rare chromosome disorders. IV. Cases 9 and 10.
    Moore MK, Engel E.
    Ann Genet; 1970 Dec 01; 13(4):269-74. PubMed ID: 5313392
    [No Abstract] [Full Text] [Related]

  • 9. [Identification of numerical and structural anomalies of human G-group-chromosomes using the pankreatin-Giemsa-Banding-pattern].
    Müller W, Rosenkranz W.
    Klin Padiatr; 1972 Jul 01; 184(4):265-71. PubMed ID: 4117041
    [No Abstract] [Full Text] [Related]

  • 10. [Ring chromosomes in mosaicism 46, XY, Cr-46, XY].
    Ferrier S, Freund M, Grétillat A.
    Arch Genet (Zur); 1973 Jul 01; 46(1):1-14. PubMed ID: 4731928
    [No Abstract] [Full Text] [Related]

  • 11. [A case of translocation t(Cp-; Bp+)].
    Ricci N, Ventimiglia B, Dallapiccola B, Preto G.
    Ann Genet; 1967 Jun 01; 10(2):82-5. PubMed ID: 5298977
    [No Abstract] [Full Text] [Related]

  • 12. [Autosomal chromosome aberrations].
    Schinzel A.
    Arch Genet (Zur); 1979 Jun 01; 52(1-2):1-204. PubMed ID: 389192
    [No Abstract] [Full Text] [Related]

  • 13. [The intelligence level in the chromosome aberrations affecting autosomes].
    Moor L.
    Rev Neuropsychiatr Infant; 1970 Dec 01; 18(12):943-66. PubMed ID: 4251821
    [No Abstract] [Full Text] [Related]

  • 14. [Autosomal chromosome aberrations].
    Serville F, Battin J.
    Bord Med; 1971 May 01; 4(5):1373-416. PubMed ID: 5105683
    [No Abstract] [Full Text] [Related]

  • 15. Quinacrine fluoromicroscopy in the identification of human mitotic chromosomes.
    Alfi OS, Donnell GN, Derencsenyi A.
    Pediatrics; 1971 Sep 01; 48(3):423-5. PubMed ID: 4255309
    [No Abstract] [Full Text] [Related]

  • 16. A cytogenetic investigation of the leukocytes of the blood of viral hepatitis patients and of blood donors.
    Dement'ev IV, Barinskii IF, Shakhgil'dyan IV, Belikova VP.
    Sov Genet; 1970 Oct 01; 6(10):1380-6. PubMed ID: 5527759
    [No Abstract] [Full Text] [Related]

  • 17. Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.
    Francke U.
    Am J Hum Genet; 1972 Mar 01; 24(2):189-213. PubMed ID: 5016511
    [No Abstract] [Full Text] [Related]

  • 18. A partial trisomy 5p syndrome.
    Opitz JM, Patau K.
    Birth Defects Orig Artic Ser; 1975 Mar 01; 11(5):191-200. PubMed ID: 1218213
    [No Abstract] [Full Text] [Related]

  • 19. Familial (13q14q) and (14q21q) translocation.
    Czerski P, Rogóyski A, Stolarska A, Wróblewska K.
    Helv Paediatr Acta; 1974 Nov 01; 29(5):443-6. PubMed ID: 4281417
    [No Abstract] [Full Text] [Related]

  • 20. A family with a presumptive C-F translocation in five generations.
    Therkelsen AJ, Klinge T, Henningsen K, Mikkelsen M, Schmidt G.
    Ann Genet; 1971 Mar 01; 14(1):13-21. PubMed ID: 5314290
    [No Abstract] [Full Text] [Related]

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