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Journal Abstract Search


460 related items for PubMed ID: 6859098

  • 1.
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  • 2. The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndrome.
    Moerman P, Fryns JP, Vandenberghe K, Devlieger H, Lauweryns JM.
    Am J Med Genet; 1988 Dec; 31(4):805-14. PubMed ID: 3239572
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  • 3. Pallister-Killian and Fryns syndromes: nosology.
    McPherson EW, Ketterer DM, Salsburey DJ.
    Am J Med Genet; 1993 Aug 15; 47(2):241-5. PubMed ID: 8213912
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  • 4. [Fryns syndrome. Report on 3 new cases].
    Alessandri JL, Attali T, Brayer C, Dupuy L, Pilorget H, Ramful D, Samperiz S, Tiran-Rajaofera I, Robin S.
    Arch Pediatr; 2007 Jul 15; 14(7):903-7. PubMed ID: 17442547
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  • 5. Fryns syndrome without diaphragmatic hernia?
    Willems PJ, Keersmaekers GH, Dom KE, Colpaert C, Schatteman E, Vergote IB, Dumon JE.
    Am J Med Genet; 1991 Nov 01; 41(2):255-7. PubMed ID: 1785645
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  • 6. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome.
    Schrander-Stumpel C, de Die-Smulders C, Fryns JP, da Costa J, Bouckaert P.
    Am J Med Genet; 1990 Sep 01; 37(1):133-5. PubMed ID: 2240030
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  • 10. Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome.
    Bamforth JS, Leonard CO, Chodirker BN, Chitayat D, Gritter HL, Evans JA, Keena B, Pantzar T, Friedman JM, Hall JG.
    Am J Med Genet; 1989 Jan 01; 32(1):93-9. PubMed ID: 2650550
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  • 13. Skeletal manifestations in Fryns syndrome.
    Tsukahara M, Sase M, Tateishi H, Saito T, Kato H, Furukawa S.
    Am J Med Genet; 1995 Jan 16; 55(2):217-20. PubMed ID: 7717421
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  • 14. Holzgreve syndrome: recurrence in sibs.
    Thomas IT, Honore GM, Jewett T, Velvis H, Garber P, Ruiz C.
    Am J Med Genet; 1993 Mar 15; 45(6):767-9. PubMed ID: 8456859
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  • 15. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies.
    Malpuech G, Demeocq F, Palcoux JB, Vanlieferinghen P.
    Am J Med Genet; 1983 Dec 15; 16(4):475-80. PubMed ID: 6660246
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  • 16. Lethal Pallister-Killian syndrome: phenotypic similarity with Fryns syndrome.
    Rodríguez JI, Garcia I, Alvarez J, Delicado A, Palacios J.
    Am J Med Genet; 1994 Nov 01; 53(2):176-81. PubMed ID: 7856644
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  • 17. Apparently new MCA/MR syndrome in sibs with cleft lip and palate and other facial, eye, heart, and intestinal anomalies.
    Kapur S, Toriello HV.
    Am J Med Genet; 1991 Dec 15; 41(4):423-5. PubMed ID: 1776630
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  • 19. Cleft-palate lateral synechia syndrome: insight into the phenotypic spectrum of Fryns syndrome?
    Jaeger A, Kapur R, Whelan M, Leung E, Cunningham M.
    Birth Defects Res A Clin Mol Teratol; 2003 Jun 15; 67(6):460-6. PubMed ID: 12962292
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  • 20. [Fryns syndrome. Description of a case].
    Ficcadenti A, Lorenzini L, Brocani P, Celani P, Kantar A, Chiaramoni L, Gabrielli O.
    Pathologica; 1993 Jun 15; 85(1096):233-9. PubMed ID: 8361787
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