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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

226 related items for PubMed ID: 2098049

  • 1.
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  • 2. Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
    Majewski E, Goecke T, Meinecke P.
    Am J Med Genet; 1996 May 03; 63(1):185-9. PubMed ID: 8723107
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  • 4. Six generations of a family with multiple limb deficiencies.
    Helal A, Perry T, Ogden JA, Greene TL.
    J Pediatr Orthop; 1993 May 03; 13(2):210-3. PubMed ID: 8459013
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  • 6. Genetics of split hand and split foot. A case study.
    Caldwell BD.
    J Am Podiatr Med Assoc; 1996 Jun 03; 86(6):244-8. PubMed ID: 8699344
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  • 7. Discrepancies in upper and lower limb patterning in split hand foot malformation.
    Elliott AM, Reed MH, Roscioli T, Evans JA.
    Clin Genet; 2005 Nov 03; 68(5):408-23. PubMed ID: 16207208
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  • 8. On the inheritance of the split hand/split foot malformation.
    Zlotogora J.
    Am J Med Genet; 1994 Oct 15; 53(1):29-32. PubMed ID: 7802032
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  • 10. Counseling dilemmas in EEC syndrome.
    Tekin M, Ohle C, Johnson DE, Christmas JT, Bodurtha J.
    Genet Couns; 2000 Oct 15; 11(1):19-24. PubMed ID: 10756423
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  • 12. A split hand-split foot (SHFM3) gene is located at 10q24-->25.
    Gurrieri F, Prinos P, Tackels D, Kilpatrick MW, Allanson J, Genuardi M, Vuckov A, Nanni L, Sangiorgi E, Garofalo G, Nunes ME, Neri G, Schwartz C, Tsipouras P.
    Am J Med Genet; 1996 Apr 24; 62(4):427-36. PubMed ID: 8723077
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  • 13. Autosomal dominant inheritance of scalp defects with ectrodactyly.
    Bonafede RP, Beighton P.
    Am J Med Genet; 1979 Apr 24; 3(1):35-41. PubMed ID: 474617
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  • 15. [A DNA duplication at chromosome 10q24.3 is associated with split-hand split-foot malformation in a Chinese family].
    Yang W, Hu ZJ, Yu XF, Li QH, Zhang AJ, Deng X, Zhang AY, Gao CS, Liu Y, Ao Y, Lo WH, Zhang X.
    Zhonghua Yi Xue Za Zhi; 2006 Mar 14; 86(10):652-8. PubMed ID: 16681918
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  • 17. Phenotypic variability of triphalangeal thumb-polysyndactyly syndrome linked to chromosome 7q36.
    Balci S, Demirtas M, Civelek B, Piskin M, Sensoz O, Akarsu AN.
    Am J Med Genet; 1999 Dec 22; 87(5):399-406. PubMed ID: 10594878
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  • 19. Phenotype and counseling in lacrimo-auriculo-dento-digital (LADD) syndrome.
    Horn D, Witkowski R.
    Genet Couns; 1993 Dec 22; 4(4):305-9. PubMed ID: 8110420
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  • 20. Congenital hand and forearm anomalies.
    Louis DS, Tsai E.
    Curr Opin Pediatr; 1996 Feb 22; 8(1):61-4. PubMed ID: 8680518
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