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Journal Abstract Search

138 related items for PubMed ID: 6823976

  • 1. Terminal deletion with stable acentric fragment of 1q in a child with congenital malformations.
    Kucerová M, Polívková Z, Dluholucký S, Kvasnicová M.
    Am J Hum Genet; 1983 Jan; 35(1):91-5. PubMed ID: 6823976
    [Abstract] [Full Text] [Related]

  • 2. Terminal long-arm deletion of chromosome 1 in a male infant.
    Dignan PS, Soukup S.
    Hum Genet; 1979 Apr 27; 48(2):151-6. PubMed ID: 457139
    [Abstract] [Full Text] [Related]

  • 3. Terminal deletion of (1)(q42) and its phenotypical manifestations.
    Andrle M, Erlach A, Mayr WR, Rett A.
    Hum Genet; 1978 Feb 23; 41(1):115-20. PubMed ID: 631857
    [Abstract] [Full Text] [Related]

  • 4. De novo 3q/7q translocation and associated interstitial 7q35 deletion.
    Fryns JP, Kleczkowska A, van den Berghe H.
    Clin Genet; 1988 Jan 23; 33(1):60-2. PubMed ID: 3342549
    [Abstract] [Full Text] [Related]

  • 5. Reproductive failure in a carrier of inv dupl l(q21.4----q12).
    Toncheva D, Genkova P, Tzoneva M, Lozanova T, Angelova E, Mitreva B.
    Acta Paediatr Hung; 1986 Jan 23; 27(1):61-6. PubMed ID: 3730184
    [Abstract] [Full Text] [Related]

  • 6. Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation.
    Franceschini P, Cirillo Silengo M, Davi G, Bianco R, Biagioli M.
    Hum Genet; 1983 Jan 23; 64(1):98. PubMed ID: 6873945
    [No Abstract] [Full Text] [Related]

  • 7. Inverted tandem duplication generates a duplication deficiency of chromosome 8p.
    Dill FJ, Schertzer M, Sandercock J, Tischler B, Wood S.
    Clin Genet; 1987 Aug 23; 32(2):109-13. PubMed ID: 2888552
    [Abstract] [Full Text] [Related]

  • 8. Monosomy 1pter.
    Yunis E, Quintero L, Leibovici M.
    Hum Genet; 1981 Aug 23; 56(3):279-82. PubMed ID: 7239511
    [No Abstract] [Full Text] [Related]

  • 9. A case of 46,XY,t(1;13) (q24;q32) with mental retardation.
    Wilbur L, Curcuru-Giordano FM, Krishna SG, Kardon NB, Jenkins EC.
    Hum Genet; 1977 Jun 30; 37(2):239-42. PubMed ID: 885541
    [Abstract] [Full Text] [Related]

  • 10. Partial deletion of 1q, following a pericentric inversion, in a boy with multiple minor morphologic anomalies and mental retardation.
    Schwanitz G, Schmid P, Hägele C, Daffner HW, Grosse KP.
    Acta Genet Med Gemellol (Roma); 1977 Jun 30; 26(2):173-5. PubMed ID: 596113
    [Abstract] [Full Text] [Related]

  • 11. A specific syndrome due to deletion of the distal long arm of chromosome 1.
    Meinecke P, Vögtel D.
    Am J Med Genet; 1987 Oct 30; 28(2):371-6. PubMed ID: 3322005
    [Abstract] [Full Text] [Related]

  • 12. Partial monosomy of long arm of chromosome 4 due to interstitial deletion.
    McDermott A, Cain R, Howell R.
    Hum Genet; 1980 Oct 30; 53(3):305-7. PubMed ID: 7372333
    [Abstract] [Full Text] [Related]

  • 13. Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21----q25) and del(1)(q41----q43).
    Beemer FA, Klep-de Pater JM, Sepers GJ, Janssen B.
    Clin Genet; 1985 May 30; 27(5):515-9. PubMed ID: 4006278
    [Abstract] [Full Text] [Related]

  • 14. Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomalies.
    Franceschini P, Cirillo Silengo M, Davi G, Bianco R, Biagioli M.
    Hum Genet; 1983 May 30; 64(1):97. PubMed ID: 6873944
    [No Abstract] [Full Text] [Related]

  • 15. De novo interstitial deletion of the long arm of chromosome 2 in a malformed newborn with a karyotype: 46,XY,del(2)(q12q14).
    Antich J, Carbonell X, Mas J, Clusellas N.
    Acta Paediatr Scand; 1983 Jul 30; 72(4):631-3. PubMed ID: 6624439
    [Abstract] [Full Text] [Related]

  • 16. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to interstitial deletion 1q.
    Steinbach P, Wolf M, Schmidt H.
    Am J Med Genet; 1984 Sep 30; 19(1):131-6. PubMed ID: 6496565
    [Abstract] [Full Text] [Related]

  • 17. 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 30; 52(2):116-9. PubMed ID: 9298747
    [Abstract] [Full Text] [Related]

  • 18. Monosomy, trisomy, fragile sites, and rearrangements of chromosome no. 1 in a mentally retarded male with multiple congenital anomalies.
    Neu RL, Kousseff BG, Madan S, Essig YP, Miller K, Tedesco TA.
    Clin Genet; 1988 Feb 30; 33(2):73-7. PubMed ID: 3359669
    [Abstract] [Full Text] [Related]

  • 19. Additional case of de novo interstitial deletion del(17)(q21.3q23) and expansion of the phenotype.
    Khalifa MM, MacLeod PM, Duncan AM.
    Clin Genet; 1993 Nov 30; 44(5):258-61. PubMed ID: 7906212
    [Abstract] [Full Text] [Related]

  • 20. Interstitial deletion of chromosome 1 (q23-q25). Report of a case.
    Silengo MC, Davi GF, Bianco R, Biagioli M, Guala A, Franceschini P, Novelli G.
    Clin Genet; 1984 Jun 30; 25(6):549-52. PubMed ID: 6587954
    [Abstract] [Full Text] [Related]

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