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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

423 related items for PubMed ID: 7039311

  • 1. The distal arthrogryposes: delineation of new entities--review and nosologic discussion.
    Hall JG, Reed SD, Greene G.
    Am J Med Genet; 1982 Feb; 11(2):185-239. PubMed ID: 7039311
    [Abstract] [Full Text] [Related]

  • 2. Limb pterygium syndromes: a review and report of eleven patients.
    Hall JG, Reed SD, Rosenbaum KN, Gershanik J, Chen H, Wilson KM.
    Am J Med Genet; 1982 Aug; 12(4):377-409. PubMed ID: 7124793
    [Abstract] [Full Text] [Related]

  • 3. Distal arthrogryposis type II: a family with varying congenital abnormalities.
    Reiss JA, Sheffield LJ.
    Am J Med Genet; 1986 Jun; 24(2):255-67. PubMed ID: 3717209
    [Abstract] [Full Text] [Related]

  • 4. Extending the spectrum of distal arthrogryposis.
    Gripp KW, Scott CI, Brockett BC, Nicholson L, Mackenzie WG.
    Am J Med Genet; 1996 Nov 11; 65(4):286-90. PubMed ID: 8923937
    [Abstract] [Full Text] [Related]

  • 5. The distal arthrogryposes: a new classification of peripheral contractures.
    Beals RK.
    Clin Orthop Relat Res; 2005 Jun 11; (435):203-10. PubMed ID: 15930940
    [Abstract] [Full Text] [Related]

  • 6. Part I. Amyoplasia: a common, sporadic condition with congenital contractures.
    Hall JG, Reed SD, Driscoll EP.
    Am J Med Genet; 1983 Aug 11; 15(4):571-90. PubMed ID: 6614047
    [Abstract] [Full Text] [Related]

  • 7. Distal arthrogryposis type 1: clinical analysis of a large kindred.
    Bamshad M, Bohnsack JF, Jorde LB, Carey JC.
    Am J Med Genet; 1996 Nov 11; 65(4):282-5. PubMed ID: 8923936
    [Abstract] [Full Text] [Related]

  • 8. Familial distal arthrogryposis type I.
    Stoll C, Alembik Y, Dott B.
    Ann Genet; 1996 Nov 11; 39(2):75-80. PubMed ID: 8766137
    [Abstract] [Full Text] [Related]

  • 9. Dominant inheritance of cleft palate with minor abnormalities of hands and feet: a new syndrome?
    Kirk EP, Wilson M.
    Clin Dysmorphol; 1999 Jul 11; 8(3):193-7. PubMed ID: 10457853
    [Abstract] [Full Text] [Related]

  • 10. Ovine heritable arthrogryposis multiplex congenita with probable lethal autosomal recessive mutation.
    Tejedor MT, Ferrer LM, Monteagudo LV, Ramos JJ, Lacasta D, Climent S.
    J Comp Pathol; 2010 Jul 11; 143(1):14-9. PubMed ID: 20153865
    [Abstract] [Full Text] [Related]

  • 11. Distinct craniofacial syndrome of lagophthalmia and bilateral cleft lip and palate.
    Korula S, Wilson L, Salomonson J.
    Am J Med Genet; 1995 Nov 06; 59(2):229-33. PubMed ID: 8588591
    [Abstract] [Full Text] [Related]

  • 12. [Congenital multiple arthrogryposis. Clinical and genetic study].
    Gallegos-Rivera M, Carnevale A, Valdés H, del Castillo V.
    Bol Med Hosp Infant Mex; 1991 Feb 06; 48(2):88-95. PubMed ID: 2054091
    [Abstract] [Full Text] [Related]

  • 13. [The Freeman-Sheldon Syndrome].
    Aldinger G, Eulert J.
    Z Orthop Ihre Grenzgeb; 1983 Feb 06; 121(5):630-3. PubMed ID: 6649811
    [Abstract] [Full Text] [Related]

  • 14. Surgical management of the hand in Freeman-Sheldon syndrome.
    Kalliainen LK, Drake DB, Edgerton MT, Grzeskiewicz JL, Morgan RF.
    Ann Plast Surg; 2003 May 06; 50(5):456-62; discussion 463-70. PubMed ID: 12792532
    [Abstract] [Full Text] [Related]

  • 15. Two brothers with distal arthrogryposis, peculiar facial appearance, cleft palate, short stature, hydronephrosis, retentio testis, and normal intelligence: a new type of distal arthrogryposis?
    Sonoda T, Kouno K.
    Am J Med Genet; 2000 Apr 10; 91(4):280-5. PubMed ID: 10766984
    [Abstract] [Full Text] [Related]

  • 16. Cleft palate, ptosis, digital anomalies and mental retardation: a new syndrome or a distal arthrogryposis variant?
    Boles RG.
    Clin Dysmorphol; 1999 Jan 10; 8(1):63-5. PubMed ID: 10327254
    [Abstract] [Full Text] [Related]

  • 17. Distal arthrogryposis type II D in three generations of a Brazilian family.
    Pagnan NA, Gollop TR.
    Am J Med Genet; 1987 Mar 10; 26(3):613-9. PubMed ID: 3565478
    [Abstract] [Full Text] [Related]

  • 18. Familial Gordon syndrome associated with a PIEZO2 mutation.
    Alisch F, Weichert A, Kalache K, Paradiso V, Longardt AC, Dame C, Hoffmann K, Horn D.
    Am J Med Genet A; 2017 Jan 10; 173(1):254-259. PubMed ID: 27714920
    [Abstract] [Full Text] [Related]

  • 19. Clinical analysis of a variant of Freeman-Sheldon syndrome (DA2B).
    Krakowiak PA, Bohnsack JF, Carey JC, Bamshad M.
    Am J Med Genet; 1998 Feb 26; 76(1):93-8. PubMed ID: 9508073
    [Abstract] [Full Text] [Related]

  • 20. Distal aphalangia, syndactyly, and extra metatarsal, associated with short stature, microcephaly, and borderline intelligence: a new autosomal dominant disorder.
    Martínez-Frías ML, Martín M, Pardo M, Fernandez de las Heras F, Frías JL.
    Am J Med Genet; 1995 Jan 16; 55(2):213-6. PubMed ID: 7717420
    [Abstract] [Full Text] [Related]

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