These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

275 related items for PubMed ID: 7367071

  • 1. [Case of chromosome X pentasomy].
    Sito A, Krzyzanowska J, Hofman H, Witkowska J, Sioch R, Mroczek-Orłow T.
    Pediatr Pol; 1980 Jan; 55(1):77-80. PubMed ID: 7367071
    [No Abstract] [Full Text] [Related]

  • 2. De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.
    Murthy DS, Murthy SK, Banker GJ, Patel AJ.
    Indian Pediatr; 1991 May; 28(5):546-9. PubMed ID: 1684352
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. [49,XXXXY syndrome in a 5-year-old boy].
    Wiśniewski L, Krajewska-Walasek M, Lech H, Mospinek M.
    Pediatr Pol; 1980 Jan; 55(1):81-6. PubMed ID: 7189276
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 7. [Chromosome 8 trisomy in an infant].
    Rogóyski A, Babel M, Tronowska TD.
    Pediatr Pol; 1982 Jan; 57(5-6):425-7. PubMed ID: 7155694
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
    Hsia YE, Appadorai V, Breg WR, Howard RO.
    Birth Defects Orig Artic Ser; 1974 Jan; 10(8):19-25. PubMed ID: 4142400
    [No Abstract] [Full Text] [Related]

  • 11. [48,XXYY syndrome in a boy with essential tremor. Comparison with 120 cases from the literature].
    Donati F, Gasser S, Mullis P, Braga S, Vassella F.
    Monatsschr Kinderheilkd; 1992 Apr; 140(4):216-9. PubMed ID: 1614446
    [Abstract] [Full Text] [Related]

  • 12. [Fetal triploidy--diagnosis and sequelae].
    Hauschild R, Beensen V, Eichhorn KH, Schulze E.
    Zentralbl Gynakol; 1991 Apr; 113(2):111-3. PubMed ID: 2042423
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. [Familial Russell-syndrome (author's transl)].
    Schwingshackl A, Ganner E, Hammerer I.
    Padiatr Padol; 1974 Apr; 9(2):130-7. PubMed ID: 4823694
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Preaxial acrofacial dysostosis (Nager syndrome) associated with an inherited and apparently balanced X;9 translocation: prenatal and postnatal late replication studies.
    Zori RT, Gray BA, Bent-Williams A, Driscoll DJ, Williams CA, Zackowski JL.
    Am J Med Genet; 1993 Jun 01; 46(4):379-83. PubMed ID: 8357008
    [Abstract] [Full Text] [Related]

  • 20. [Ring chromosome 18. 18p-/18q- -deletion-syndrome].
    Kunze J, Stephan E, Tolksdorf M.
    Humangenetik; 1972 Jun 01; 15(4):289-318. PubMed ID: 4565746
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.