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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

208 related items for PubMed ID: 9375923

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  • 3. Imperforate anus in Feingold syndrome.
    Büttiker V, Wojtulewicz J, Wilson M.
    Am J Med Genet; 2000 May 29; 92(3):166-9. PubMed ID: 10817649
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  • 5. Vertebral anomalies in a new family with ODED syndrome.
    Piersall LD, Dowton SB, McAlister WH, Waggoner DJ.
    Clin Genet; 2000 Jun 29; 57(6):444-8. PubMed ID: 10905665
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  • 7. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay.
    Feingold M, Hall BD, Lacassie Y, Martínez-Frías ML.
    Am J Med Genet; 1997 Mar 31; 69(3):245-9. PubMed ID: 9096752
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  • 8. Growth deficiency in oculodigitoesophagoduodenal (Feingold) syndrome--case report and review of the literature.
    Shaw-Smith C, Willatt L, Thalange N.
    Clin Dysmorphol; 2005 Jul 31; 14(3):155-158. PubMed ID: 15930908
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  • 10. Feingold syndome: a rare but important cause of syndromic tracheoesophageal fistula.
    Layman-Pleet L, Jackson CC, Chou S, Boycott KM.
    J Pediatr Surg; 2007 Sep 31; 42(9):E1-3. PubMed ID: 17848225
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  • 13. MODED: microcephaly-oculo-digito-esophageal-duodenal syndrome.
    Frydman M, Katz M, Cabot SG, Soen G, Kauschansky A, Sirota L.
    Am J Med Genet; 1997 Aug 22; 71(3):251-7. PubMed ID: 9268091
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  • 14. Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies.
    Innis JW, Asher JH, Poznanski AK, Sheldon S.
    Am J Med Genet; 1997 Aug 08; 71(2):150-5. PubMed ID: 9217213
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  • 15. Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype.
    Tedesco MG, Lonardo F, Ceccarini C, Cesarano C, Digilio MC, Magliozzi M, Rogaia D, Mencarelli A, Leoni C, Piscopo C, Imperatore V, Falco MT, Fontana P, Nardone AM, Novelli A, Troiani S, Seri M, Prontera P.
    Am J Med Genet A; 2021 Apr 08; 185(4):1204-1210. PubMed ID: 33442900
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  • 17. How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?
    Ravel A, Chouery E, Stora S, Jalkh N, Villard L, Temtamy S, Mégarbané A.
    Am J Med Genet A; 2011 Apr 08; 155A(4):880-4. PubMed ID: 21416592
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  • 20. Hand-foot-genital syndrome: the importance of hallux varus.
    Cleveland RH, Holmes LB.
    Pediatr Radiol; 1990 Apr 08; 20(5):339-43. PubMed ID: 2349017
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