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Journal Abstract Search

239 related items for PubMed ID: 8042668

  • 1. Scalp-ear-nipple syndrome: additional manifestations.
    Edwards MJ, McDonald D, Moore P, Rae J.
    Am J Med Genet; 1994 Apr 15; 50(3):247-50. PubMed ID: 8042668
    [Abstract] [Full Text] [Related]

  • 2. Hypothelia, syndactyly, and ear malformation--a variant of the scalp-ear-nipple syndrome?: Case report and review of the literature.
    Baris H, Tan WH, Kimonis VE.
    Am J Med Genet A; 2005 Apr 15; 134A(2):220-2. PubMed ID: 15712197
    [Abstract] [Full Text] [Related]

  • 3. Unusual manifestations of ectodermal dysplasia-syndactyly syndrome type I in two Yemeni siblings.
    Mohammad A.
    Dermatol Online J; 2015 Jan 15; 21(1):. PubMed ID: 25612123
    [Abstract] [Full Text] [Related]

  • 4. Aplasia cutis congenita associated with syndactyly and supernumerary nipples: report of a second family with similar clinical findings.
    Halper S, Rubenstein D.
    Pediatr Dermatol; 1991 Mar 15; 8(1):32-4. PubMed ID: 1650463
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Scalp-Ear-Nipple syndrome: first report of a Potassium channel tetramerization domain-containing 1 in-frame insertion and review of the literature.
    Butler KM, Bahrambeigi V, Merrihew A, Friez MJ, Cathey SS.
    Clin Dysmorphol; 2021 Oct 01; 30(4):167-172. PubMed ID: 34456244
    [Abstract] [Full Text] [Related]

  • 7. Aplasia cutis congenita, congenital heart lesions, and frontonasal cysts in four successive generations.
    Rodrigues RG.
    Clin Genet; 2007 Jun 01; 71(6):558-60. PubMed ID: 17539905
    [Abstract] [Full Text] [Related]

  • 8. Autosomal recessive ectodermal dysplasia, cleft lip/palate, mental retardation, and syndactyly: the Zlotogora-Ogur syndrome.
    Rodini ES, Richieri-Costa A.
    Am J Med Genet; 1990 Aug 01; 36(4):473-6. PubMed ID: 2167611
    [Abstract] [Full Text] [Related]

  • 9. [Hair collar sign associated with scalp aplasia cutis congenita].
    Roche-Gamón E, Febrer-Bosch I, Alegre de Miquel V.
    Actas Dermosifiliogr; 2007 Aug 01; 98(6):442-3. PubMed ID: 17663938
    [No Abstract] [Full Text] [Related]

  • 10. Brief clinical report: new, autosomal dominant form of ectodermal dysplasia.
    Tuffli GA, Laxova R.
    Am J Med Genet; 1983 Feb 01; 14(2):381-4. PubMed ID: 6837633
    [Abstract] [Full Text] [Related]

  • 11. Mutations in KCTD1 cause scalp-ear-nipple syndrome.
    Marneros AG, Beck AE, Turner EH, McMillin MJ, Edwards MJ, Field M, de Macena Sobreira NL, Perez AB, Fortes JA, Lampe AK, Giovannucci Uzielli ML, Gordon CT, Plessis G, Le Merrer M, Amiel J, Reichenberger E, Shively KM, Cerrato F, Labow BI, Tabor HK, Smith JD, Shendure J, Nickerson DA, Bamshad MJ, University of Washington Center for Mendelian Genomics.
    Am J Hum Genet; 2013 Apr 04; 92(4):621-6. PubMed ID: 23541344
    [Abstract] [Full Text] [Related]

  • 12. [The Adams-Oliver syndrome in Spain: the epidemiological aspects].
    Martínez-Frías ML, Arroyo Carrera I, Muñoz-Delgado NJ, Nieto Conde C, Rodríguez-Pinilla E, Urioste Azcorra M, Omeñaca Teres F, García Alix A.
    An Esp Pediatr; 1996 Jul 04; 45(1):57-61. PubMed ID: 8849132
    [Abstract] [Full Text] [Related]

  • 13. Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: another case of Finlay-Marks syndrome.
    Plessis G, Le Treust M, Le Merrer M.
    Clin Genet; 1997 Oct 04; 52(4):231-4. PubMed ID: 9383029
    [Abstract] [Full Text] [Related]

  • 14. An hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples.
    Finlay AY, Marks R.
    Br J Dermatol; 1978 Oct 04; 99(4):423-30. PubMed ID: 708615
    [Abstract] [Full Text] [Related]

  • 15. Scalp-ear-nipple (Finlay-Marks) syndrome: a familial case with renal involvement.
    Picard C, Couderc S, Skojaei T, Salomon R, de Lonlay P, Le Merrer M, Munnich A, Lyonnet S, Amiel J.
    Clin Genet; 1999 Aug 04; 56(2):170-2. PubMed ID: 10517259
    [No Abstract] [Full Text] [Related]

  • 16. Aplasia cutis congenita of the scalp, skull and dura associated with Adams-Oliver syndrome.
    Bilginer B, Onal MB, Bahadir S, Akalan N.
    Turk Neurosurg; 2008 Apr 04; 18(2):191-3. PubMed ID: 18597236
    [Abstract] [Full Text] [Related]

  • 17. Finlay-Marks syndrome: report of two siblings and review of literature.
    Naik P, Kini P, Chopra D, Gupta Y.
    Am J Med Genet A; 2012 Jul 04; 158A(7):1696-701. PubMed ID: 22639454
    [Abstract] [Full Text] [Related]

  • 18. Terminal transverse defects with aplasia cutis congenita (Adams-Oliver syndrome).
    Shapiro SD, Escobedo MK.
    Birth Defects Orig Artic Ser; 1985 Jul 04; 21(2):135-42. PubMed ID: 4041576
    [No Abstract] [Full Text] [Related]

  • 19. Scalp defect, nipples absence and ears abnormalities: an other case of Finlay syndrome.
    Le Merrer M, Renier D, Briard ML.
    Genet Couns; 1991 Jul 04; 2(4):233-6. PubMed ID: 1799422
    [Abstract] [Full Text] [Related]

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