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Journal Abstract Search

143 related items for PubMed ID: 1415344

  • 1. Ophthalmological, skeletal, and cardiac abnormalities in sibs born to consanguineous parents: a new syndrome?
    dos Santos Rde C, Castro NH, Ferraz OP, Walter-Moura J, Mustachi Z, Pagnan NA, Gollop TR.
    Am J Med Genet; 1992 Aug 01; 43(6):946-8. PubMed ID: 1415344
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  • 2. Anterior segment anomalies of the eye, clefting and skeletal abnormalities in two sibs of consanguineous parents: Michels syndrome or new syndrome?
    al Gazali LI, al Talabani J, Mosawi A, Lytle W.
    Clin Dysmorphol; 1994 Jul 01; 3(3):238-44. PubMed ID: 7981860
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  • 3. Anterior segment anomalies of the eye associated with multiple skeletal abnormalities and early lethality: confirmation of an autosomal recessive syndrome.
    al-Gazali LI, Bakir M, Sadaghatian MR, Nath R, Haas D.
    Clin Dysmorphol; 1999 Apr 01; 8(2):87-92. PubMed ID: 10319196
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  • 6. Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family.
    Arnold GL, Bixler D, Girod D.
    Am J Med Genet; 1983 Sep 01; 16(1):35-42. PubMed ID: 6638068
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  • 7. Brief clinical report: autosomal recessive anophthalmia with multiple congenital abnormalities--type Waardenburg.
    Richieri-Costa A, Gollop TR, Otto PG.
    Am J Med Genet; 1983 Apr 01; 14(4):607-15. PubMed ID: 6846395
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  • 10. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B, Ulmer H, Müller U.
    Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348
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  • 12. Fraser syndrome with renal agenesis in two consanguineous Turkish families.
    Francannet C, Lefrançois P, Dechelotte P, Robert E, Malpuech G, Robert JM.
    Am J Med Genet; 1990 Aug 01; 36(4):477-9. PubMed ID: 2389805
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  • 13. Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant.
    Franceschini P, Testa A, Bogetti G, Girardo E, Guala A, Lopez-Bell G, Buzio G, Ferrario E, Piccato E.
    Am J Med Genet; 1992 Jan 01; 42(1):112-6. PubMed ID: 1308349
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  • 14. Ophthalmo-acromelic syndrome.
    Le Merrer M, Nessmann C, Briard ML, Maroteaux P.
    Ann Genet; 1988 Jan 01; 31(4):226-9. PubMed ID: 3146242
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  • 16. A new autosomal recessive disorder resembling Weaver syndrome.
    Teebi AS, Sundareshan TS, Hammouri MY, al-Awadi SA, al-Saleh QA.
    Am J Med Genet; 1989 Aug 01; 33(4):479-82. PubMed ID: 2596508
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  • 18. Michels syndrome in a Brazilian girl born to consanguineous parents.
    Guion-Almeida ML, Rodini ES.
    Am J Med Genet; 1995 Jul 03; 57(3):377-9. PubMed ID: 7677137
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  • 19. Two siblings with midline field defects and Hirschsprung disease: variable expression of Toriello-Carey or new syndrome?
    Jespers A, Buntinx I, Melis K, Vaerenberg M, Janssens G.
    Am J Med Genet; 1993 Aug 15; 47(2):299-302. PubMed ID: 8213924
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  • 20. Lethal faciocardiomelic dysplasia- a new autosomal recessive disorder.
    Cantú JM, Hernández A, Ramírez J, Bernal M, Rubio G, Urrusti J, Franco-Vázquez S.
    Birth Defects Orig Artic Ser; 1975 Aug 15; 11(5):91-8. PubMed ID: 1218241
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