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Journal Abstract Search

156 related items for PubMed ID: 3901750

  • 41. Distal 12p deletion in a stillborn infant.
    Baroncini A, Avellini C, Neri C, Forabosco A.
    Am J Med Genet; 1990 Jul; 36(3):358-60. PubMed ID: 2363438
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  • 42. [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
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  • 43. [Del (13) (q33). Exclusion of esterase D (ESD) from 13q33 and q34].
    Turleau C, Séger J, de Grouchy J, Doré F, Job JC.
    Ann Genet; 1978 Sep; 21(3):189-92. PubMed ID: 315197
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  • 44. Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12).
    Gonzalez CH, Billerbeck AE, Takayama LC, Wajntal A.
    Am J Med Genet; 1983 Jan; 14(1):159-67. PubMed ID: 6829605
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  • 45. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
    Cousineau AJ, Higgins JV, Scott-Emuakpor AB, Mody G.
    Am J Med Genet; 1983 Jan; 14(1):29-35. PubMed ID: 6829609
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  • 46. Terminal deletion of 6p: report of a new case.
    Plaja A, Vidal R, Soriano D, Bou X, Vendrell T, Mediano C, Pueyo JM, Labraña X, Sarret E.
    Ann Genet; 1994 Jan; 37(4):196-9. PubMed ID: 7710255
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  • 47. Leiomyoma of uterus in a patient with ring chromosome 12: case presentation and literature review.
    Hajianpour MJ, Hajianpour AK, Habibian R, Wohlmuth C.
    Am J Med Genet; 1996 May 17; 63(2):335-9. PubMed ID: 8725781
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  • 48. Cytogenetic abnormalities in two new patients with Pitt-Rogers-Danks phenotype.
    Lindeman-Kusse MC, Van Haeringen A, Hoorweg-Nijman JJ, Brunner HG.
    Am J Med Genet; 1996 Dec 02; 66(1):104-12. PubMed ID: 8957526
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  • 49. Clinical and molecular cytogenetic studies in ring chromosome 5: report of a child with congenital abnormalities.
    Basinko A, Giovannucci Uzielli ML, Scarselli G, Priolo M, Timpani G, De Braekeleer M.
    Eur J Med Genet; 2012 Feb 02; 55(2):112-6. PubMed ID: 22193390
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  • 50. Exclusion of glutathione reductase from 8pter leads to 8p22 and localization to 8p21.
    Magenis RE, Reiss J, Bigley R, Chamberlin J, Lovrien E.
    Cytogenet Cell Genet; 1978 Feb 02; 22(1-6):446-8. PubMed ID: 752521
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  • 52. [Partial deletion of the short arm of chromosome 3. Report of a case (author's transl)].
    Gonzales J, Lesourd S, Braconnier A.
    Ann Genet; 1980 Feb 02; 23(2):119-22. PubMed ID: 6967285
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  • 56. Hereditary spherocytic anemia with deletion of the short arm of chromosome 8.
    Okamoto N, Wada Y, Nakamura Y, Nakayama M, Chiyo H, Murayama K, Inoue T, Kanzaki A, Yawata Y, Hirono A.
    Am J Med Genet; 1995 Sep 11; 58(3):225-9. PubMed ID: 8533822
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  • 58. Constitutional interstitial deletion of 17(p11.2) (Smith-Magenis syndrome): a clinically recognizable microdeletion syndrome. Report of two cases and review of the literature.
    Fischer H, Oswald HP, Duba HC, Doczy L, Simma B, Utermann G, Haas OA.
    Klin Padiatr; 1993 Sep 11; 205(3):162-6. PubMed ID: 8350589
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