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Journal Abstract Search

165 related items for PubMed ID: 5141271

  • 1. The branchio-skeleto-genital syndrome. A new hereditary syndrome.
    el-Sahy NI, Waters WR.
    Plast Reconstr Surg; 1971 Dec; 48(6):542-50. PubMed ID: 5141271
    [No Abstract] [Full Text] [Related]

  • 2. Cranio-facial and dental anomalies in the Branchio-Skeleto-Genital (BSG) syndrome with suggestions for more appropriate nomenclature.
    Wedgwood DL, Curran JB, Lavelle CL, Trott JR.
    Br J Oral Surg; 1983 Jun; 21(2):94-102. PubMed ID: 6575818
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  • 3. Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance.
    Dallaire L.
    J Med Genet; 1969 Jun; 6(2):113-20. PubMed ID: 4389828
    [No Abstract] [Full Text] [Related]

  • 4. The hypertelorism-hypospadias syndrome.
    Reed MH, Shokeir MH, Macpherson RI.
    J Can Assoc Radiol; 1975 Dec; 26(4):240-8. PubMed ID: 1223121
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  • 5. [Branchio-skeleto-genital syndrome].
    Ishii T.
    Ryoikibetsu Shokogun Shirizu; 2001 Dec; (33):297-8. PubMed ID: 11462446
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  • 9. A novel deletion in a Pearson syndrome infant with hypospadias and cleft lip and palate.
    Lohi O, Kuusela AL, Arola M.
    J Inherit Metab Dis; 2005 Dec; 28(6):1165-6. PubMed ID: 16435219
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  • 10. The radiology of Coffin-Lowry syndrome.
    Padley S, Hodgson SV, Sherwood T.
    Br J Radiol; 1990 Jan; 63(745):72-5. PubMed ID: 2306591
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  • 11. The W syndrome. Studies of malformation syndromes of man XXVIII.
    Pallister PD, Herrmann J, Spranger JW, Gorlin RJ, Langer LO, Opitz JM.
    Birth Defects Orig Artic Ser; 1974 Jan; 10(7):51-60. PubMed ID: 4425540
    [No Abstract] [Full Text] [Related]

  • 12. An autosomal dominant syndrome of uveal colobomata, cleft lip and palate, and mental retardation.
    Kingston HM, Harper PS, Jones PW.
    J Med Genet; 1982 Dec; 19(6):444-6. PubMed ID: 7154042
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  • 13. Two brothers with characteristic facial appearance, severe psychomotor retardation, hypospadias, contractures, and other symptoms: a new recessive syndrome?
    Wolff G, Zimmermann E, Zimmerhackl B, Harnasch C, Jung C, Back E.
    J Med Genet; 1994 Jan; 31(1):65-7. PubMed ID: 8151642
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  • 14. Schilbach-Rott syndrome in a third family: further delineation of an autosomal dominant trait.
    Becerra-Solano LE, Casillas-Avila MP, Díaz-Rodríguez M, Nastasi-Catanese JA, Toscano-Flores JJ, Ramírez-Dueñas ML.
    Genet Couns; 2007 Jan; 18(3):317-23. PubMed ID: 18019373
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  • 18. Unusual facies, cleft palate, mental retardation, and limb abnormalities in siblings--a new syndrome.
    Palant DI, Feingold M, Berkman MD.
    J Pediatr; 1971 Apr; 78(4):686-9. PubMed ID: 5547829
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  • 19. Hereditary vitreoretinal degeneration, cleft lip and palate, deafness, and skeletal dysplasia.
    Regenbogen L, Godel V.
    Am J Ophthalmol; 1980 Mar; 89(3):414-8. PubMed ID: 6966133
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