These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

146 related items for PubMed ID: 20717165

  • 1. Type II familial synpolydactyly: report on two families with an emphasis on variations of expression.
    Al-Qattan MM.
    Eur J Hum Genet; 2011 Jan; 19(1):112-4. PubMed ID: 20717165
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?
    Akarsu AN, Akhan O, Sayli BS, Sayli U, Baskaya G, Sarfarazi M.
    J Med Genet; 1995 Jun; 32(6):435-41. PubMed ID: 7666394
    [Abstract] [Full Text] [Related]

  • 4. Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I?
    Percin EF, Percin S, Egilmez H, Sezgin I, Ozbas F, Akarsu AN.
    J Med Genet; 1998 Oct; 35(10):868-74. PubMed ID: 9783716
    [Abstract] [Full Text] [Related]

  • 5. Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndrome.
    Lohan S, Spielmann M, Doelken SC, Flöttmann R, Muhammad F, Baig SM, Wajid M, Hülsemann W, Habenicht R, Kjaer KW, Patil SJ, Girisha KM, Abarca-Barriga HH, Mundlos S, Klopocki E.
    Clin Genet; 2014 Oct; 86(4):318-25. PubMed ID: 24456159
    [Abstract] [Full Text] [Related]

  • 6. Synpolydactyly (type II syndactyly) with aplasia/hypoplasia of the middle phalanges of the toes: report on a family with eight affected members in four generations.
    Camera G, Camera A, Pozzolo S, Costa M, Mantero R.
    Am J Med Genet; 1995 Jan 16; 55(2):244-6. PubMed ID: 7717427
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. An unusual family with brachydactyly.
    Silva EO.
    Am J Med Genet A; 2003 Mar 01; 117A(2):191-3. PubMed ID: 12567422
    [No Abstract] [Full Text] [Related]

  • 9. 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
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. A novel type of autosomal recessive syndactyly: clinical and molecular studies in a family of Pakistani origin.
    Malik S, Arshad M, Amin-Ud-Din M, Oeffner F, Dempfle A, Haque S, Koch MC, Ahmad W, Grzeschik KH.
    Am J Med Genet A; 2004 Apr 01; 126A(1):61-7. PubMed ID: 15039974
    [Abstract] [Full Text] [Related]

  • 13. Congenital hypoplastic anemia in six patients: unusual association of short proximal phalanges with mild anemia.
    Cetin M, Kara A, Gürgey A, Gümrük F, Irken G, Yetgin S, Altay C.
    Pediatr Hematol Oncol; 1995 Apr 01; 12(2):153-8. PubMed ID: 7626383
    [Abstract] [Full Text] [Related]

  • 14. [Genetic analysis of a Chinese pedigree with congenital synpolydactyly].
    Qin W, Shu AL, Xing QH, Yang MS, Feng GY, He L.
    Yi Chuan Xue Bao; 2003 Oct 01; 30(10):973-7. PubMed ID: 14669516
    [Abstract] [Full Text] [Related]

  • 15. Complex Camptosynpolydactyly and Mesoaxial synostotic syndactyly with phalangeal reduction are allelic disorders.
    Phadke SR, Kar A, Bhowmik AD, Dalal A.
    Am J Med Genet A; 2016 Jun 01; 170(6):1622-5. PubMed ID: 27041388
    [Abstract] [Full Text] [Related]

  • 16. Sandrow syndrome of mirror hands and feet and facial abnormalities.
    Kogekar N, Teebi AS, Vockley J.
    Am J Med Genet; 1993 Apr 15; 46(2):126-8. PubMed ID: 8387243
    [Abstract] [Full Text] [Related]

  • 17. [Synpolydactyly: unusual features and variable expression in 5 generations of an Italian family].
    Chessa Ricotti G, Lapi E, De Bernardi A, Corti P.
    Pediatr Med Chir; 1990 Apr 15; 12(3):259-63. PubMed ID: 2177188
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Are triphalangeal thumb-polysyndactyly syndrome (TPTPS) and tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome (THPTTS) identical? A father with TPTPS and his daughter with THPTTS in a Thai family.
    Kantaputra PN, Chalidapong P.
    Am J Med Genet; 2000 Jul 17; 93(2):126-31. PubMed ID: 10869115
    [Abstract] [Full Text] [Related]

  • 20. A and B preaxial polydactyly with syndactyly of feet and hands in the same person--a case report.
    Gawlikowska-Sroka A, Tudaj W, Czerwiński F.
    Adv Med Sci; 2009 Jul 17; 54(2):305-7. PubMed ID: 20053619
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.