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

372 related items for PubMed ID: 9298747

  • 1. Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient.
    Caliebe A, Waltz S, Jenderny J.
    Clin Genet; 1997 Aug; 52(2):116-9. PubMed ID: 9298747
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 4. Interstitial deletion of the short arm of chromosome 4.
    Ray M, Evans J, Rockman-Greenberg C, Wickstrom D.
    J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
    [Abstract] [Full Text] [Related]

  • 5. Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15).
    Stoll C, Levy J, Roth MP.
    J Med Genet; 1980 Dec; 17(6):486-7. PubMed ID: 7205434
    [Abstract] [Full Text] [Related]

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

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

  • 8. New case of interstitial deletion 12(q15-q21.2) in a girl with facial dysmorphism and mental retardation.
    Schluth C, Gesny R, Borck G, Redon R, Abadie V, Kleinfinger P, Munnich A, Lyonnet S, Colleaux L.
    Am J Med Genet A; 2008 Jan 01; 146A(1):93-6. PubMed ID: 18076123
    [Abstract] [Full Text] [Related]

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

  • 10. Rieger syndrome and interstitial 4q26 deletion.
    Fryns JP, Van Den Berghe H.
    Genet Couns; 1992 Jan 01; 3(3):153-4. PubMed ID: 1388934
    [No Abstract] [Full Text] [Related]

  • 11. A familial "balanced" 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings.
    Wagstaff J, Hemann M.
    Am J Hum Genet; 1995 Jan 01; 56(1):302-9. PubMed ID: 7825591
    [Abstract] [Full Text] [Related]

  • 12. 16q21 is critical for 16q deletion syndrome.
    Naritomi K, Shiroma N, Izumikawa Y, Sameshima K, Ohdo S, Hirayama K.
    Clin Genet; 1988 May 01; 33(5):372-5. PubMed ID: 3378367
    [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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. 46, XY, del (3) (pter-->p25) syndrome: further delineation of the clinical phenotype.
    Benini D, Vino L, Vecchini S, Fanos V.
    Eur J Pediatr; 1999 Dec 01; 158(12):955-7. PubMed ID: 10592068
    [Abstract] [Full Text] [Related]

  • 19. [A new clinico-cytogenetic syndrome--a proximal deletion of the short arm of chromosome 17].
    Zaletaev DV, Marincheva GS.
    Pediatriia; 1988 Dec 01; (11):82-4. PubMed ID: 3226810
    [No Abstract] [Full Text] [Related]

  • 20. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
    Piovani G, Borsani G, Bertini V, Kalscheuer VM, Viertel P, Bellotti D, Valseriati D, Barlati S.
    Eur J Med Genet; 2006 Dec 01; 49(3):215-23. PubMed ID: 16762823
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 19.