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Journal Abstract Search

237 related items for PubMed ID: 4141590

  • 1. A peculiar t(21 ; 14) translocation, associated with a pericentric inversion of the Y chromosome in a mongol boy.
    Orye E, Verhaaren H.
    Ann Genet; 1974 Sep; 17(3):217-20. PubMed ID: 4141590
    [No Abstract] [Full Text] [Related]

  • 2. Structural variation in human nitotic chromosomes.
    Leisti J.
    Ann Acad Sci Fenn Biol; 1971 Sep; 179():1-69. PubMed ID: 4261167
    [No Abstract] [Full Text] [Related]

  • 3. [Familial pericentric inversion of y chromosome and Down's syndrome].
    García Sagredo JM, Morán Cabré A, San Román Cos-Gayón C.
    An Esp Pediatr; 1975 Sep; 8(1):68-71. PubMed ID: 123717
    [Abstract] [Full Text] [Related]

  • 4. [Infant with free trisomy 21 and maternal t(14q 22q) translocation].
    Forabosco A, Dutrillaux B, Toni G, Lejeune J.
    Ann Genet; 1973 Mar; 16(1):57-9. PubMed ID: 4269148
    [No Abstract] [Full Text] [Related]

  • 5. [Pericentric inversion of a chromosome 21. Study of 3 generations. Genetic counseling].
    Fraisse J.
    J Genet Hum; 1975 Oct; 23 SUPPL():107-11. PubMed ID: 129537
    [No Abstract] [Full Text] [Related]

  • 6. Updating advances in cytogenetics. Applications of the new chromosome banding methods.
    Breg WR.
    Birth Defects Orig Artic Ser; 1974 Oct; 10(8):7-18. PubMed ID: 4142402
    [No Abstract] [Full Text] [Related]

  • 7. [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; 184(4):265-71. PubMed ID: 4117041
    [No Abstract] [Full Text] [Related]

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

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  • 14. [Functional analysis of chromosome translocation (DqGq) in hereditary Down's syndrome by DNA replication pattern].
    Abe T.
    Saishin Igaku; 1968 Feb 10; 24(2):313-6. PubMed ID: 4239275
    [No Abstract] [Full Text] [Related]

  • 15. [Familial occurrence of translocation (13q 14q) and 14q 21q)].
    Czerski P, Rogóyski A, Stolarska A.
    Pediatr Pol; 1977 Apr 10; 52(4):429-35. PubMed ID: 141033
    [No Abstract] [Full Text] [Related]

  • 16. Trisomy and D/G translocation mongolism in brothers.
    Ingalls TH, Henry TA.
    N Engl J Med; 1968 Jan 04; 278(1):10-4. PubMed ID: 4229204
    [No Abstract] [Full Text] [Related]

  • 17. [Significance of chromosome translocations from the G-D group in the karyotype of the mother of 2 children with Down's syndrome].
    Dobrzańska A, Kostrzewski J.
    Pediatr Pol; 1970 Feb 04; 45(2):211-5. PubMed ID: 4245096
    [No Abstract] [Full Text] [Related]

  • 18. [Down's syndrome with G/G "tandem" translocation (author's transl)].
    López Pajares I, Barreiro E, Delicado A.
    An Esp Pediatr; 1976 Feb 04; 9(5):553-7. PubMed ID: 136915
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  • 19. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV, Prozorova MV, Khitrikova LE.
    Tsitol Genet; 1984 Feb 04; 18(3):223-8. PubMed ID: 6235655
    [Abstract] [Full Text] [Related]

  • 20. [Quantitative multienzymatic deficiency and chromosome malsegregation: patients with trisomy 21 and their parents].
    Grozdea J, Colombies P, Verdier J.
    Nouv Presse Med; 1973 May 12; 2(19):1289-91. PubMed ID: 4268234
    [No Abstract] [Full Text] [Related]

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