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Journal Abstract Search

223 related items for PubMed ID: 8010352

  • 1. Vohwinkel syndrome (mutilating keratoderma) associated with craniofacial anomalies.
    Sensi A, Bettoli V, Zampino MR, Gandini E, Calzolari E.
    Am J Med Genet; 1994 Apr 01; 50(2):201-3. PubMed ID: 8010352
    [Abstract] [Full Text] [Related]

  • 2. A new variant of Vohwinkel syndrome: a case report.
    Seirafi H, Khezri S, Morowati S, Kamyabhesari K, Mirzaeipour M, Khezri F.
    Dermatol Online J; 2011 Mar 15; 17(3):3. PubMed ID: 21426869
    [Abstract] [Full Text] [Related]

  • 3. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness.
    Sommer A, Young-Wee T, Frye T.
    Am J Med Genet; 1983 May 15; 15(1):71-7. PubMed ID: 6859126
    [Abstract] [Full Text] [Related]

  • 4. Parameters for evaluation and treatment of patients with cleft lip/palate or other craniofacial anomalies. American Cleft Palate-Craniofacial Association. March, 1993.
    Cleft Palate Craniofac J; 1993 Mar 15; 30 Suppl():S1-16. PubMed ID: 8457579
    [No Abstract] [Full Text] [Related]

  • 5. [Papillon-Lefévre syndrome. Report of a case with association of campto, clinodactylia and cranial anomalies].
    Fonseca Capdevila E, Soto Melo J, Santamaría Solís L, Maza León P.
    Actas Dermosifiliogr; 1980 Mar 15; 71(5-6):237-40. PubMed ID: 6451148
    [No Abstract] [Full Text] [Related]

  • 6. [Associated malformations of the head and extremities].
    Tridon P.
    J Genet Hum; 1974 Dec 15; 22(4):365-80. PubMed ID: 4282383
    [No Abstract] [Full Text] [Related]

  • 7. G59S mutation in the GJB2 gene in a Chinese family with classic Vohwinkel syndrome.
    Xie MX, Yang WP, Luo HJ, Ismail F, Hao YY, Yang JQ.
    J Dermatol; 2019 Feb 15; 46(2):154-157. PubMed ID: 30565282
    [Abstract] [Full Text] [Related]

  • 8. The value of establishing the genetic component in etiology of craniofacial anomalies.
    Stewart RE.
    Birth Defects Orig Artic Ser; 1980 Feb 15; 16(5):27-33. PubMed ID: 7448376
    [No Abstract] [Full Text] [Related]

  • 9. Frontonasal dysplasia (median cleft face syndrome): comments on etiology and pathogenesis.
    Cohen MM, Sedano HO, Gorlin RJ, Jirásek JE.
    Birth Defects Orig Artic Ser; 1971 Jun 15; 7(7):117-9. PubMed ID: 5173199
    [No Abstract] [Full Text] [Related]

  • 10. Striate palmoplantar keratoderma in a patient with Rubinstein-Taybi syndrome.
    Nakai K, Yoneda K, Moriue T, Kubota Y.
    J Eur Acad Dermatol Venereol; 2009 Mar 15; 23(3):333-5. PubMed ID: 18637050
    [No Abstract] [Full Text] [Related]

  • 11. An apparently new acrocraniofacial syndrome with cranial nerve and visceral anomalies.
    Hameed R, Bissenden JG, Webb WR, Cole TR.
    Clin Dysmorphol; 1999 Jul 15; 8(3):199-202. PubMed ID: 10457854
    [Abstract] [Full Text] [Related]

  • 12. Craniofacial clefts.
    Thorne CH.
    Clin Plast Surg; 1993 Oct 15; 20(4):803-14. PubMed ID: 8275642
    [Abstract] [Full Text] [Related]

  • 13. Median facial malformations and their implications for brain malformations.
    DeMyer W.
    Birth Defects Orig Artic Ser; 1975 Oct 15; 11(7):155-81. PubMed ID: 764897
    [Abstract] [Full Text] [Related]

  • 14. [Complex partial seizures in a case of Vohwinkel syndrome (keratoma hereditaria mutilans)].
    Martínez Castrillo JC, Medina S, Gobernado Serrano J.
    Neurologia; 1992 Jan 15; 7(1):39. PubMed ID: 1534485
    [No Abstract] [Full Text] [Related]

  • 15. Cleft lip and palate, characteristic facial appearance, malrotation of the intestine, and lethal congenital heart disease in two sibs: a new autosomal recessive condition?
    McPherson E, Clemens M.
    Am J Med Genet; 1996 Mar 01; 62(1):58-60. PubMed ID: 8779326
    [Abstract] [Full Text] [Related]

  • 16. Vohwinkel syndrome with mental retardation.
    Mercy P, Singh A, Ghorpade AK, Das MN, Upadhyay A, Keswani N.
    Indian J Dermatol Venereol Leprol; 2013 Mar 01; 79(5):725. PubMed ID: 23974601
    [No Abstract] [Full Text] [Related]

  • 17. [Chromosomal studies in craniofacial abnormalities].
    Ahrens K.
    HNO; 1967 Apr 01; 15(4):106-9. PubMed ID: 5592377
    [No Abstract] [Full Text] [Related]

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