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Journal Abstract Search

187 related items for PubMed ID: 5347076

  • 21. A newborn with the cat-eye syndrome.
    Fryns JP, Eggermont E, Veresen H, Van den Berghe H.
    Humangenetik; 1972; 15(3):242-8. PubMed ID: 5082091
    [No Abstract] [Full Text] [Related]

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  • 25. Autosomal translocation in a mentally retarded male child with 46,XY,t(2q-;13q+) complement. Case report and review.
    Genest P, Lachance R, Poty J, Jacob D.
    J Med Genet; 1971 Dec; 8(4):504-8. PubMed ID: 5149534
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  • 28. Ring chromosomes in two infants with congenital malformations.
    Varela MA, Sternberg WH.
    J Med Genet; 1969 Sep; 6(3):334-41. PubMed ID: 5345107
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  • 31. Inherited chromosomal translocation in two families (t(4q-;13q+) and t(5q-; 13q+)).
    Watanabe G, Kiyoi Y, Takeyama I, Kawana S, Yamamoto M.
    Tohoku J Exp Med; 1977 Feb; 121(2):179-84. PubMed ID: 847744
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  • 32. [Clinical diagnosis of the phenotype corresponding to a ring-shaped D chromosome].
    Rethoré MO, Praud E, Le Loc'h J, Joly C, Saraux H, Aussannaire M, Lejeune J.
    Presse Med (1893); 1970 Apr 25; 78(21):955-8. PubMed ID: 4986088
    [No Abstract] [Full Text] [Related]

  • 33. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.
    Butler LJ, Eades SM, France NE.
    Ann Genet; 1969 Mar 25; 12(1):15-27. PubMed ID: 5306708
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  • 34. [Trisomy D2 in a 2 and one-half year old girl (47,XX,14+)].
    Murken JD, Bauchinger M, Palitzsch D, Pfeifer H, Suschke J, Haendle H.
    Humangenetik; 1970 Mar 25; 10(3):254-68. PubMed ID: 5475510
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  • 35. [Deletion of the short arm of chromosome 4].
    Berger R.
    Nouv Presse Med; 1972 Mar 18; 1(12):809-10. PubMed ID: 5015459
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  • 36. Trisomy 13 with a 13q14q translocation.
    Coco R, Penchaszadeh B.
    J Genet Hum; 1975 Mar 18; 23(1):1-6. PubMed ID: 1165477
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  • 37. Human chromosomal deletion: two patients with the 4p- syndrome.
    Arias D, Passarge E, Engle MA, German J.
    J Pediatr; 1970 Jan 18; 76(1):82-8. PubMed ID: 5410164
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  • 38. New chromosomal syndromes.
    Lewandowski RC, Yunis JJ.
    Am J Dis Child; 1975 Apr 18; 129(4):515-29. PubMed ID: 124130
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  • 39. A case of a girl with a 21 ring chromosome.
    Kucerová M, Polívková Z.
    Hum Hered; 1974 Apr 18; 24(1):100-4. PubMed ID: 4136482
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  • 40. CHROMOSOMAL AUTORADIOGRAPHY IN THE CRI DU CHAT SYNDROME.
    GERMAN J, LEJEUNE J, MACINTYRE MN, DE GROUCHY J.
    Cytogenetics; 1964 Apr 18; 3():347-52. PubMed ID: 14248464
    [No Abstract] [Full Text] [Related]

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