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Journal Abstract Search

157 related items for PubMed ID: 872834

  • 21.
    ; . PubMed ID:
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  • 22. Tetra-phocomelia with multiple malformations: X-linked amelia, or Roberts syndrome, or DK-phocomelia syndrome?
    Rodríguez JI, Palacios J, Urioste M, Rodríguez-Peralto JL.
    Am J Med Genet; 1992 Jun 01; 43(3):630-2. PubMed ID: 1605264
    [No Abstract] [Full Text] [Related]

  • 23. Roberts syndrome with normal cell division.
    Keppen LD, Gollin SM, Seibert JJ, Sisken JE.
    Am J Med Genet; 1991 Jan 01; 38(1):21-4. PubMed ID: 2012128
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  • 24. The Roberts syndrome/SC phocomelia spectrum--a case report of an adult with review of the literature.
    Goh ES, Li C, Horsburgh S, Kasai Y, Kolomietz E, Morel CF.
    Am J Med Genet A; 2010 Feb 01; 152A(2):472-8. PubMed ID: 20101700
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  • 27. Tetra-amelia with lung hypoplasia and facial clefts, Roberts-SC syndrome: report of two cases.
    Ragavan M, Reddy S, Kumar C.
    Pediatr Surg Int; 2010 Oct 01; 26(10):1049-52. PubMed ID: 20625748
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  • 31. Incidental detection of premature centromere separation in amniocytes associated with a mild form of Roberts syndrome.
    Stanley WS, Pai GS, Horger EO, Yan YS, McNeal KS.
    Prenat Diagn; 1988 Oct 01; 8(8):565-9. PubMed ID: 3205861
    [Abstract] [Full Text] [Related]

  • 32. [The Roberts-SC phocomelia syndrome. Apropos of a case without cytogenetic changes and review of the literature].
    López-Herce J, Rodríguez Sánchez C, Duelo M, Fontoura M, González M, Gracia R, Oliver A, Peralta A.
    An Esp Pediatr; 1985 Dec 01; 23(8):588-92. PubMed ID: 3006564
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  • 33.
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  • 36. [Roberts-SC phocomelia syndrome].
    Baggio P, Danda R, Audino G.
    Pediatr Med Chir; 1986 Dec 01; 8(1):115-9. PubMed ID: 3725603
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  • 37. [Case of cytomegalovirus infection and phocomelia].
    Gatniejewska-Komraus M, Bońkowski A.
    Pediatr Pol; 1979 May 01; 54(5):515-8. PubMed ID: 223114
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  • 38. Syndrome of multiple congenital malformations including phocomelia, thrombocytopenia, encephalocele, and urogenital abnormalities.
    Cherstvoy E, Lazjuk G, Lurie I, Ostrovskaya T, Shved I.
    Lancet; 1980 Aug 30; 2(8192):485. PubMed ID: 6106133
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  • 40. LADD syndrome in five members of a three-generation family and prenatal diagnosis.
    Francannet C, Vanlieferinghen P, Dechelotte P, Urbain MF, Campagne D, Malpuech G.
    Genet Couns; 1994 Aug 30; 5(1):85-91. PubMed ID: 8031542
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