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Journal Abstract Search

91 related items for PubMed ID: 8092192

  • 1. Deletion 5q35.3.
    Stratton RF, Tedrowe NA, Tolworthy JA, Patterson RM, Ryan SG, Young RS.
    Am J Med Genet; 1994 Jun 01; 51(2):150-2. PubMed ID: 8092192
    [Abstract] [Full Text] [Related]

  • 2. Interstitial deletion of the long arm of chromosome 11: report of a case and review of the literature.
    Wakazono A, Masuno M, Yamaguchi S, Tsubouchi K, Kondo N, Orii T.
    Jpn J Hum Genet; 1992 Sep 01; 37(3):229-34. PubMed ID: 1472705
    [Abstract] [Full Text] [Related]

  • 3. Terminal deletion 1q43 in a newborn with hydrocephalus.
    Ribeiro MC, Brunoni D.
    Ann Genet; 1987 Sep 01; 30(2):126-8. PubMed ID: 3499845
    [Abstract] [Full Text] [Related]

  • 4. Infant with multiple congenital anomalies and deletion (9)(q34.3).
    Schimmenti LA, Berry SA, Tuchman M, Hirsch B.
    Am J Med Genet; 1994 Jun 01; 51(2):140-2. PubMed ID: 7522397
    [Abstract] [Full Text] [Related]

  • 5. De novo 10q22 interstitial deletion.
    Cook L, Weaver DD, Hartsfield JK, Vance GH.
    J Med Genet; 1999 Jan 01; 36(1):71-2. PubMed ID: 9950372
    [Abstract] [Full Text] [Related]

  • 6. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
    Sukumar S, Wang S, Hoang K, Vanchiere CM, England K, Fick R, Pagon B, Reddy KS.
    Am J Med Genet; 1999 Nov 05; 87(1):17-22. PubMed ID: 10528241
    [Abstract] [Full Text] [Related]

  • 7. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
    Zenger-Hain JL, Roberson J, Van Dyke DL, Weiss L.
    Am J Med Genet; 1993 Jun 01; 46(4):438-40. PubMed ID: 7689299
    [Abstract] [Full Text] [Related]

  • 8. Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins(8;5)(p23;q33q35).
    Gibbons B, Tan SY, Kee SK, Quaife R, Lim ST.
    Am J Med Genet; 1999 Sep 17; 86(3):289-93. PubMed ID: 10482883
    [Abstract] [Full Text] [Related]

  • 9. Interstitial deletion of chromosome 18[del(18)(q11.2q12.2 or q12.2q21.1].
    Surh LC, Ledbetter DH, Greenberg F.
    Am J Med Genet; 1991 Oct 01; 41(1):15-7. PubMed ID: 1719812
    [Abstract] [Full Text] [Related]

  • 10. [18 short arm deletion. Report of one case (author's transl)].
    Barreiro E, Delicado A, López Pajares I, Cordero L, Junco E, Castroviejo IP.
    An Esp Pediatr; 1977 Jan 01; 10(1):112-7. PubMed ID: 842972
    [Abstract] [Full Text] [Related]

  • 11. Molecular cytogenetic analysis of a de novo interstitial deletion of 5q23.3q31.2 and its phenotypic consequences.
    Tzschach A, Krause-Plonka I, Menzel C, Kalscheuer V, Toennies H, Scherthan H, Knoblauch A, Radke M, Ropers HH, Hoeltzenbein M.
    Am J Med Genet A; 2006 Mar 01; 140(5):496-502. PubMed ID: 16470790
    [Abstract] [Full Text] [Related]

  • 12. A case with de novo interstitial deletion of chromosome 7q21.1-q22.
    Manguoğlu E, Berker-Karaüzüm S, Baumer A, Mihçi E, Taçoy S, Lüleci G, Schinzel A.
    Genet Couns; 2005 Mar 01; 16(2):155-9. PubMed ID: 16080295
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb 01; 26(2):138-46. PubMed ID: 16470734
    [Abstract] [Full Text] [Related]

  • 14. Chromosome 5q subtelomeric deletion syndrome.
    Rauch A, Dörr HG.
    Am J Med Genet C Semin Med Genet; 2007 Nov 15; 145C(4):372-6. PubMed ID: 17910075
    [Abstract] [Full Text] [Related]

  • 15. New syndrome of macrocephaly, hypertelorism, short limbs, hearing loss, and developmental delay.
    Bagatelle R, Cassidy SB.
    Am J Med Genet; 1995 Jan 30; 55(3):367-71. PubMed ID: 7537019
    [Abstract] [Full Text] [Related]

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  • 17. Interstitial deletion of chromosome 2 region in a malformed infant.
    Melnyk AR, Muraskas J.
    Am J Med Genet; 1993 Jan 01; 45(1):49-51. PubMed ID: 8418659
    [Abstract] [Full Text] [Related]

  • 18.
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  • 19. Interstitial deletion of bands 11q21-->22.3 in a three-year-old girl defined using fluorescence in situ hybridization on metaphase chromosomes.
    Horelli-Kuitunen N, Gahmberg N, Eeva M, Palotie A, Järvelä I.
    Am J Med Genet; 1999 Oct 29; 86(5):416-9. PubMed ID: 10508981
    [Abstract] [Full Text] [Related]

  • 20. Terminal deletion of the long arm of chromosome 2 in a premature infant with karyotype: 46,XY,del(2)(q37).
    Wang TH, Johnston K, Hsieh CL, Dennery PA.
    Am J Med Genet; 1994 Feb 15; 49(4):399-401. PubMed ID: 8160733
    [Abstract] [Full Text] [Related]

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