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PUBMED FOR HANDHELDS

Journal Abstract Search

185 related items for PubMed ID: 526587

  • 1. Variable expression in otopalatodigital syndrome; cleft palate in female.
    Salinas CF, Jorgenson RJ, Lorenzo RL.
    Birth Defects Orig Artic Ser; 1979; 15(5B):329-45. PubMed ID: 526587
    [No Abstract] [Full Text] [Related]

  • 2. Distraction in a case of otopalatodigital syndrome type II.
    Batra P, Ryan FS, Witherow H, Calvert ML.
    Int J Paediatr Dent; 2006 Jul; 16(4):286-91. PubMed ID: 16759327
    [Abstract] [Full Text] [Related]

  • 3. Autosomal dominant asymmetrical radial dysplasia, dysmorphic facies, and conductive hearing loss (facioauriculoradial dysplasia).
    Harding AE, Hall CM, Baraitser M.
    J Med Genet; 1982 Apr; 19(2):110-5. PubMed ID: 7077621
    [Abstract] [Full Text] [Related]

  • 4. Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome. Its association with conductive hearing loss.
    Robinson GC, Wildervanck LS, Chiang TP.
    J Pediatr; 1973 Jan; 82(1):107-9. PubMed ID: 4681851
    [No Abstract] [Full Text] [Related]

  • 5. Dominant inheritance of multiple epiphyseal dysplasia, myopia and deafness.
    Beighton P, Goldberg L, Hof JO.
    Clin Genet; 1978 Sep; 14(3):173-7. PubMed ID: 699354
    [Abstract] [Full Text] [Related]

  • 6. The otopalatodigital (OPD) syndrome: (conductive deafness, cleft palate and anomaly of digits).
    Nager GT, Char F.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):273-4. PubMed ID: 5173224
    [No Abstract] [Full Text] [Related]

  • 7. Conductive deafness with ptosis and skeletal malformations in sibs: a probably autosomal recessive disorder.
    Jackson LG, Barr MA.
    Birth Defects Orig Artic Ser; 1978 Jun; 14(6B):199-204. PubMed ID: 728561
    [No Abstract] [Full Text] [Related]

  • 8. Proximal symphalangia and stapes ankylosis.
    Cremers C, Theunissen E, Kuijpers W.
    Arch Otolaryngol; 1985 Nov; 111(11):765-7. PubMed ID: 4051868
    [Abstract] [Full Text] [Related]

  • 9.
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  • 10. Camptodactyly, cleft palate, and club foot. A syndrome showing the autosomal-dominant pattern of inheritance.
    Gordon H, Davies D, Berman M.
    J Med Genet; 1969 Sep; 6(3):266-74. PubMed ID: 5345097
    [No Abstract] [Full Text] [Related]

  • 11. New skeletal dysplasia with unique brachydactyly.
    Mononen TK, Karnes PS, Senac MO, Falk RE.
    Am J Med Genet; 1992 Mar 01; 42(5):706-13. PubMed ID: 1632443
    [Abstract] [Full Text] [Related]

  • 12. Conductive deafness, symphalangism, and facial abnormalities: the WL syndrome in a Japanese family.
    Higashi K, Inoue S.
    Am J Med Genet; 1983 Sep 01; 16(1):105-9. PubMed ID: 6638061
    [Abstract] [Full Text] [Related]

  • 13. [The delta phalanx].
    Csorba E.
    Magy Traumatol Orthop Helyreallito Seb; 1987 Sep 01; 30(2):103-9. PubMed ID: 2884354
    [No Abstract] [Full Text] [Related]

  • 14. Polydactyly: a study of four generations of a Turkish family including an affected member with bilateral cleft lip and palate.
    Koçer U, Aksoy HM, Tiftikcioğlu YO, Karaaslan O.
    Scand J Plast Reconstr Surg Hand Surg; 2002 Sep 01; 36(5):284-8. PubMed ID: 12477087
    [Abstract] [Full Text] [Related]

  • 15. An autosomal dominant inherited syndrome with congenital stapes ankylosis.
    Teunissen B, Cremers WR.
    Laryngoscope; 1990 Apr 01; 100(4):380-4. PubMed ID: 2319886
    [Abstract] [Full Text] [Related]

  • 16. [Oto-palato-digital syndrome, type I].
    Narahara K.
    Ryoikibetsu Shokogun Shirizu; 2001 Apr 01; (34 Pt 2):444-5. PubMed ID: 11528828
    [No Abstract] [Full Text] [Related]

  • 17. Ectrodactyly, cleft lip and palate in two half sibs.
    Lewis MB, Pashayan HM.
    J Med Genet; 1981 Oct 01; 18(5):394-6. PubMed ID: 7328620
    [Abstract] [Full Text] [Related]

  • 18. Otopalatodigital syndrome: radiologic findings in the hand and foot.
    Poznanski AK, Macpherson RI, Dijkman DJ, Gorlin RJ, Gall JC, Stern AM, Garn SM, Nagy JM.
    Birth Defects Orig Artic Ser; 1974 Oct 01; 10(5):125-39. PubMed ID: 4469976
    [No Abstract] [Full Text] [Related]

  • 19. ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia.
    Propping P, Zerres K.
    Am J Med Genet; 1993 Mar 01; 45(5):642-8. PubMed ID: 8456838
    [Abstract] [Full Text] [Related]

  • 20.
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