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Journal Abstract Search

282 related items for PubMed ID: 4073121

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

  • 2. A chromosome 1q44 deletion in a 4-month-old girl; The first report in Korea.
    Cho JH, Song ES, Kim HN, Oh BS, Choi YY.
    Korean J Pediatr; 2014 Jun; 57(6):292-6. PubMed ID: 25076975
    [Abstract] [Full Text] [Related]

  • 3. [Distal 1q monosomy. 2 new cases and description of the syndrome].
    Turleau C, de Grouchy J, Frézal J, Richardet JM.
    Ann Genet; 1983 Jun; 26(3):161-4. PubMed ID: 6606378
    [Abstract] [Full Text] [Related]

  • 4. Further delineation of the dup(3q) syndrome.
    Wilson GN, Dasouki M, Barr M.
    Am J Med Genet; 1985 Sep; 22(1):117-23. PubMed ID: 4050847
    [Abstract] [Full Text] [Related]

  • 5. Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)].
    Al-Awadi SA, Farag TI, Usha R, el-Khalifa MY, Sundareshan TS, Al-Othman SA.
    Am J Med Genet; 1986 Apr; 23(4):931-3. PubMed ID: 3963055
    [Abstract] [Full Text] [Related]

  • 6. The 18p- syndrome. Report of five cases.
    Zumel RM, Darnaude MT, Delicado A, Diaz de Bustamante A, de Torres ML, López-Pájares I.
    Ann Genet; 1989 Apr; 32(3):160-3. PubMed ID: 2817777
    [Abstract] [Full Text] [Related]

  • 7. Chromosome 10qter deletion syndrome: a review and report of three new cases.
    Wulfsberg EA, Weaver RP, Cunniff CM, Jones MC, Jones KL.
    Am J Med Genet; 1989 Mar; 32(3):364-7. PubMed ID: 2658586
    [Abstract] [Full Text] [Related]

  • 8. A specific syndrome due to deletion of the distal long arm of chromosome 1.
    Meinecke P, Vögtel D.
    Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005
    [Abstract] [Full Text] [Related]

  • 9.
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  • 10. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
    Taysi K, Dengler DR, Jones LA, Heersma JR.
    Ann Genet; 1981 Oct; 24(4):245-7. PubMed ID: 7036843
    [No Abstract] [Full Text] [Related]

  • 11. Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.
    Lin AE, Garver KL, Diggans G, Clemens M, Wenger SL, Steele MW, Jones MC, Israel J.
    Am J Med Genet; 1988 Nov; 31(3):533-48. PubMed ID: 3067575
    [Abstract] [Full Text] [Related]

  • 12. Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.
    Obregon MG, Mingarelli R, Digilio MC, Zelante L, Giannotti A, Sabatino G, Dallapiccola B.
    Ann Genet; 1992 Nov; 35(4):208-12. PubMed ID: 1296516
    [Abstract] [Full Text] [Related]

  • 13. [Syndrome of terminal deletion of the long arm of chromosome 4. Apropos of a personal case with a review of the literature].
    Frappaz D, Bourgeois J, Berthier JC, Laurent C, Bethenod M.
    Pediatrie; 1983 Jun; 38(4):261-70. PubMed ID: 6353348
    [Abstract] [Full Text] [Related]

  • 14. Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3.
    Narahara K, Kikkawa K, Murakami M, Hiramoto K, Namba H, Tsuji K, Yokoyama Y, Kimoto H.
    Am J Med Genet; 1990 Feb; 35(2):269-73. PubMed ID: 2178418
    [Abstract] [Full Text] [Related]

  • 15.
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  • 16. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS, Gibson L, McGrath J, Meyn MS, Breg WR, Yang-Feng TL.
    Am J Med Genet; 1993 May 15; 46(3):288-92. PubMed ID: 8488873
    [Abstract] [Full Text] [Related]

  • 17. Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndrome.
    Ioan DM, Maximilian C, Kleczkowska A, Fryns JP.
    Ann Genet; 1992 May 15; 35(3):167-9. PubMed ID: 1466567
    [Abstract] [Full Text] [Related]

  • 18. Report of two cases of distal deletion of the long arm of chromosome 6.
    Stevens CA, Fineman RM, Breg WR, Silken AB.
    Am J Med Genet; 1988 Apr 15; 29(4):807-14. PubMed ID: 3400725
    [Abstract] [Full Text] [Related]

  • 19. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J, Plaza J, Geán E.
    An Esp Pediatr; 1981 Nov 15; 15(5):469-73. PubMed ID: 7332149
    [Abstract] [Full Text] [Related]

  • 20. Terminal deletion 1q43 in a newborn with hydrocephalus.
    Ribeiro MC, Brunoni D.
    Ann Genet; 1987 Nov 15; 30(2):126-8. PubMed ID: 3499845
    [Abstract] [Full Text] [Related]

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