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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

207 related items for PubMed ID: 2591402

  • 21.
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  • 22. Rectal atresia as rare manifestation in EEC syndrome.
    Majewski F, Goecke T.
    Am J Med Genet; 1996 May 03; 63(1):190-2. PubMed ID: 8723108
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  • 24. Human HOX gene mutations.
    Goodman FR, Scambler PJ.
    Clin Genet; 2001 Jan 03; 59(1):1-11. PubMed ID: 11206481
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  • 25. Six generations of a family with multiple limb deficiencies.
    Helal A, Perry T, Ogden JA, Greene TL.
    J Pediatr Orthop; 1993 Jan 03; 13(2):210-3. PubMed ID: 8459013
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  • 30. Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27.
    van Bokhoven H, Jung M, Smits AP, van Beersum S, Rüschendorf F, van Steensel M, Veenstra M, Tuerlings JH, Mariman EC, Brunner HG, Wienker TF, Reis A, Ropers HH, Hamel BC.
    Am J Hum Genet; 1999 Feb 03; 64(2):538-46. PubMed ID: 9973291
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  • 31. Cooks syndrome: a case report and brief review.
    Brennan CB, Buehler T, Lesher JL.
    Pediatr Dermatol; 2013 Feb 03; 30(4):e52-3. PubMed ID: 22329539
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  • 34. Ectrodactyly with fibular aplasia: a separate entity?
    Menke LA, Bijlsma EK, van Essen AJ, van den Boogaard MJ, van Rijn RR, Cobben JM.
    Eur J Med Genet; 2008 Feb 03; 51(5):488-96. PubMed ID: 18547886
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  • 36. Mirror hands and feet with a distinct nasal defect, an autosomal dominant condition.
    Martin RA, Jones MC, Jones KL.
    Am J Med Genet; 1993 Apr 15; 46(2):129-31. PubMed ID: 8387244
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  • 37. A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation.
    Khan S, Basit S, Zimri FK, Ali N, Ali G, Ansar M, Ahmad W.
    Clin Genet; 2012 Jul 15; 82(1):48-55. PubMed ID: 21554266
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  • 39. Congenital heart defects, hamartomas of the tongue and polysyndactyly in a sister and brother.
    Orstavik KH, Lindemann R, Solberg LA, Foerster A, Sørland SJ.
    Clin Genet; 1992 Jul 15; 42(1):19-21. PubMed ID: 1516223
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  • 40. Counseling dilemmas in EEC syndrome.
    Tekin M, Ohle C, Johnson DE, Christmas JT, Bodurtha J.
    Genet Couns; 2000 Jul 15; 11(1):19-24. PubMed ID: 10756423
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