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Journal Abstract Search

170 related items for PubMed ID: 3681906

  • 1. Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental retardation.
    Ohdo S, Madokoro H, Sonoda T, Takei M, Yasuda H, Mori N.
    J Med Genet; 1987 Oct; 24(10):609-12. PubMed ID: 3681906
    [Abstract] [Full Text] [Related]

  • 2. New autosomal recessive form of amelia.
    Michaud J, Filiatrault D, Dallaire L, Lambert M.
    Am J Med Genet; 1995 Mar 27; 56(2):164-7. PubMed ID: 7625439
    [Abstract] [Full Text] [Related]

  • 3. [Roberts-SC phocomelia syndrome].
    Musfeld DA, Bühler EM, Heinzl S.
    Gynakol Geburtshilfliche Rundsch; 2001 Mar 27; 41(1):3-7. PubMed ID: 11423730
    [Abstract] [Full Text] [Related]

  • 4. [Genetic morphological fatal syndromes. The Fryns syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Mar 27; 14(2):92-3. PubMed ID: 8469652
    [No Abstract] [Full Text] [Related]

  • 5. Further delineation of the Yunis-Varon syndrome.
    Hennekam RC, Vermeulen-Meiners C.
    J Med Genet; 1989 Jan 27; 26(1):55-8. PubMed ID: 2918527
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  • 7. An autosomal recessive ectodermal dysplasia syndrome of hypotrichosis, onychodysplasia, hyperkeratosis, kyphoscoliosis, catartact, and other manifestations.
    Alves AF, dos Santos PA, Castelo-Branco-Neto E, Freire-Maia N.
    Am J Med Genet; 1981 Jan 27; 10(3):213-8. PubMed ID: 7304669
    [Abstract] [Full Text] [Related]

  • 8. Two brothers with characteristic facial appearance, severe psychomotor retardation, hypospadias, contractures, and other symptoms: a new recessive syndrome?
    Wolff G, Zimmermann E, Zimmerhackl B, Harnasch C, Jung C, Back E.
    J Med Genet; 1994 Jan 27; 31(1):65-7. PubMed ID: 8151642
    [Abstract] [Full Text] [Related]

  • 9. A new syndrome with distinct facial and auricular malformations and dominant inheritance.
    Simosa V, Penchaszadeh VB, Bustos T.
    Am J Med Genet; 1989 Feb 27; 32(2):184-6. PubMed ID: 2929657
    [Abstract] [Full Text] [Related]

  • 10. Tetra-amelia and lung hypo/aplasia syndrome: new case report and review.
    Sousa SB, Pina R, Ramos L, Pereira N, Krahn M, Borozdin W, Kohlhase J, Amorim M, Gonnet K, Lévy N, Carreira IM, Couceiro AB, Saraiva JM.
    Am J Med Genet A; 2008 Nov 01; 146A(21):2799-803. PubMed ID: 18837045
    [Abstract] [Full Text] [Related]

  • 11. Trichorrhexis nodosa and lip pits in autosomal dominant ectodermal dysplasia--central nervous system malformation syndrome.
    Silengo M, Pietragalla A, Jarre L.
    Am J Med Genet; 1997 Aug 08; 71(2):226-8. PubMed ID: 9217228
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  • 13. Natural history and postmortem anatomy of a patient with tetra-amelia, ectodermal dysplasia, peculiar face, and developmental retardation (MIM 273390).
    Ohdo S, Sonoda T, Ohba K.
    J Med Genet; 1994 Dec 08; 31(12):980-1. PubMed ID: 7534355
    [No Abstract] [Full Text] [Related]

  • 14. A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasia: evidence for autosomal recessive inheritance.
    Fryns JP, Moerman P.
    Genet Couns; 1998 Dec 08; 9(1):61-2. PubMed ID: 9555592
    [No Abstract] [Full Text] [Related]

  • 15. Autosomal recessive neurodegenerative disorder with trichorrhexis invaginata and ectodermal dysplasia.
    Gyure KA, Kurczynski TW, Gunning W, French BN.
    Pediatr Neurol; 1992 Dec 08; 8(6):469-72. PubMed ID: 1476579
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  • 18. Hypohidrotic ectodermal dysplasia, central nervous system malformation, and distinct facial features: confirmation of a distinct entity?
    Soekarman D, Fryns JP.
    J Med Genet; 1993 Mar 08; 30(3):245-7. PubMed ID: 8474109
    [Abstract] [Full Text] [Related]

  • 19. Syndactyly, ectodermal dysplasia, and cleft lip/palate.
    Zlotogora J.
    J Med Genet; 1994 Dec 08; 31(12):957-9. PubMed ID: 7891379
    [No Abstract] [Full Text] [Related]

  • 20. Cardio-facio-cutaneous (CFC) syndrome in a child carrying an inherited inversion of chromosome 7.
    Lopez-Rangel E, Hrynchak M, Friedman JM.
    Am J Med Genet; 1993 Sep 01; 47(3):326-9. PubMed ID: 8135275
    [Abstract] [Full Text] [Related]

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