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Journal Abstract Search

211 related items for PubMed ID: 10911531

  • 1. [Feingold syndrome].
    Alessandri JL, Graber D, Tiran-Rajaofera I, Montbrun A, Pilorget H, Samperiz S, Attali T, de Napoli-Cocci S.
    Arch Pediatr; 2000 Jun; 7(6):637-40. PubMed ID: 10911531
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Feingold syndrome: report of a new family and review.
    Courtens W, Levi S, Verbelen F, Verloes A, Vamos E.
    Am J Med Genet; 1997 Nov 28; 73(1):55-60. PubMed ID: 9375923
    [Abstract] [Full Text] [Related]

  • 4. A Feingold syndrome case with previously undescribed features and a new mutation.
    Koçak H, Ozaydin E, Köse G, Marcelis CL, Kamsteeg EJ, Ceylaner S.
    Genet Couns; 2009 Nov 28; 20(3):261-7. PubMed ID: 19852433
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Feingold syndrome: clinical review and genetic mapping.
    Celli J, van Bokhoven H, Brunner HG.
    Am J Med Genet A; 2003 Nov 01; 122A(4):294-300. PubMed ID: 14518066
    [Abstract] [Full Text] [Related]

  • 7. Expanding the phenotype of feingold syndrome-2.
    Grote LE, Repnikova EA, Amudhavalli SM.
    Am J Med Genet A; 2015 Dec 01; 167A(12):3219-25. PubMed ID: 26360630
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. A new syndrome with cardiac malformation, cleft lip-palate, microcephaly and digital anomalies?
    Perçin EF, Düzcan F, Kafali G, Sezgin I.
    Clin Genet; 1995 Nov 08; 48(5):264-7. PubMed ID: 8825606
    [Abstract] [Full Text] [Related]

  • 10. Digital anomalies, microcephaly, and normal intelligence: new syndrome or Feingold syndrome?
    Kawame H, Pagon RA, Hudgins L.
    Am J Med Genet; 1997 Mar 31; 69(3):240-4. PubMed ID: 9096751
    [Abstract] [Full Text] [Related]

  • 11. Familial syndromic duodenal atresia: Feingold syndrome.
    Holder-Espinasse M, Ahmad Z, Hamill J, Pahari A, Misra D, Drake D, Winter RM, Wilson LC.
    Eur J Pediatr Surg; 2004 Apr 31; 14(2):112-6. PubMed ID: 15185158
    [Abstract] [Full Text] [Related]

  • 12. 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 31; 155A(4):880-4. PubMed ID: 21416592
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Vertebral defects in a patient with Feingold syndrome.
    Kellermayer R, Weisenbach J, Gyuris P, Aszmann M, Kosztolányi G.
    Clin Dysmorphol; 2005 Oct 31; 14(4):213-214. PubMed ID: 16155427
    [No Abstract] [Full Text] [Related]

  • 15. Pure 9p duplication syndrome with aplasia of the middle phalanges of the fifth fingers.
    Sato A, Suzuki T, Ikeno M, Takeda J, Yamamoto Y, Shinohara M, Makino S, Takeda S, Shimizu T, Itakura A.
    Eur J Med Genet; 2020 Oct 31; 63(10):104005. PubMed ID: 32693209
    [Abstract] [Full Text] [Related]

  • 16. Brachydactylic multiple delta phalanges plus syndrome.
    Ahn CP, Lachman RS, Cox VA, Blumberg B, Klein OD.
    Am J Med Genet A; 2005 Sep 15; 138(1):41-4. PubMed ID: 16092122
    [Abstract] [Full Text] [Related]

  • 17. Brachydactyly with absence of middle phalanges and hypoplastic nails. A new hereditary syndrome.
    Cuevas-Sosa A, García-Segur F.
    J Bone Joint Surg Br; 1971 Feb 15; 53(1):101-5. PubMed ID: 4325377
    [No Abstract] [Full Text] [Related]

  • 18. [Familial syndrome of microcephaly with oculocutaneous albinism and digital anomalies].
    Castro-Gago M, Pombo M, Novo I, Tojo R, Peña J.
    An Esp Pediatr; 1983 Aug 15; 19(2):128-31. PubMed ID: 6660641
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 185(4):1204-1210. PubMed ID: 33442900
    [Abstract] [Full Text] [Related]

  • 20. Humoral immunodeficiency with facial dysmorphology and limb anomalies: a new syndrome.
    Hoffman HM, Bastian JF, Bird LM.
    Clin Dysmorphol; 2001 Jan 15; 10(1):1-8. PubMed ID: 11152140
    [Abstract] [Full Text] [Related]

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