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

136 related items for PubMed ID: 1233411

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

  • 2. Radiological findings in two sisters with trisomy of the short arm of chromosome 4.
    Giovannelli G, Rossi L, Forabosco A.
    Helv Paediatr Acta; 1973 Dec; 28(6):543-52. PubMed ID: 4785152
    [No Abstract] [Full Text] [Related]

  • 3. Radiological features of the most common autosomal disorders: trisomy 21-22 (mongolism or Down's syndrome), trisomy 18, trisomy 13-15, and the cri du chat syndrome.
    James AE, Merz T, Janower ML, Dorst JP.
    Clin Radiol; 1971 Oct; 22(4):417-33. PubMed ID: 4257566
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. [Skeletal malformations caused by chromosome aberrations. Clinical and radiological study].
    Dallapiccola B, Pistocchi GF.
    Minerva Med; 1972 Dec 22; 63(92):5049-208. PubMed ID: 4264793
    [No Abstract] [Full Text] [Related]

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

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Radiologic findings in the evaluation of the common autosomal disorders.
    Berdon WE.
    Dev Med Child Neurol; 1972 Apr 22; 14(2):226-7. PubMed ID: 4260516
    [No Abstract] [Full Text] [Related]

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

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.
    Chen CP, Chen M, Su YN, Tsai FJ, Chern SR, Hsu CY, Wu PC, Town DD, Lee DJ, Ma GC, Wang W.
    Taiwan J Obstet Gynecol; 2010 Sep 22; 49(3):320-6. PubMed ID: 21056318
    [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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [Pericentric inversion of chromosome 4 : inv (4) (p13, q35) and trisomy of the short branch of chromosome 4 due to recombination aneusomy].
    Dallapiccola B, Capra L, Preto G, Covic M, Dutrillaux B.
    Ann Genet; 1974 Jun 22; 17(2):115-8. PubMed ID: 4547938
    [No Abstract] [Full Text] [Related]

  • 19. [Chromosome 8 : complete trisomy and segmental trisomies].
    Rethoré MO, Aurias A, Couturier J, Dutrillaux B, Prieur M, Lejeune J.
    Ann Genet; 1977 Mar 22; 20(1):5-11. PubMed ID: 302674
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.