These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 668970)

  • 21. Congenital ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis: a new genodermatosis?
    Lestringant GG; Küster W; Frossard PM; Happle R
    Am J Med Genet; 1998 Jan; 75(2):186-9. PubMed ID: 9450882
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome.
    van Steensel MA; van Geel M; Nahuys M; Smitt JH; Steijlen PM
    J Invest Dermatol; 2002 Apr; 118(4):724-7. PubMed ID: 11918723
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Woolly hair in 4 members of a Chinese family.
    Chen C; LeBoit PE; Price VH
    J Am Acad Dermatol; 2006 Jan; 54(1):165-6. PubMed ID: 16384778
    [No Abstract]   [Full Text] [Related]  

  • 24. Autosomal dominant lamellar ichthyosis: a new skin disorder.
    Traupe H; Kolde G; Happle R
    Clin Genet; 1984 Nov; 26(5):457-61. PubMed ID: 6499258
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Craniosynostosis, telecanthus, scalp hair abnormalities, and sensorineural deafness in two sibs.
    Mégarbané A; Hersh JH; Chouery E; Fabre M
    Am J Med Genet; 2002 May; 109(4):323-7. PubMed ID: 11992488
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Bilateral sensorineural deafness and hydrocephalus due to foramen of Monro obstruction in sibs: a newly described autosomal recessive disorder.
    Chudley AE; McCullough C; McCullough DW
    Am J Med Genet; 1997 Jan; 68(3):350-6. PubMed ID: 9024571
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Ichthyosis, follicular atrophoderma, and hypotrichosis caused by mutations in ST14 is associated with impaired profilaggrin processing.
    Alef T; Torres S; Hausser I; Metze D; Türsen U; Lestringant GG; Hennies HC
    J Invest Dermatol; 2009 Apr; 129(4):862-9. PubMed ID: 18843291
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype.
    Avrahami L; Maas S; Pasmanik-Chor M; Rainshtein L; Magal N; Smitt J; van Marle J; Shohat M; Basel-Vanagaite L
    Clin Genet; 2008 Jul; 74(1):47-53. PubMed ID: 18445049
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Ichthyosis vulgaris, growth retardation, hair dysplasia, tooth abnormalities, immunologic deficiencies, psychomotor retardation and resorption disorders. Case report of 2 siblings].
    Braun-Falco O; Ring J; Butenandt O; Selzle D; Landthaler M
    Hautarzt; 1981 Feb; 32(2):67-74. PubMed ID: 7228665
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A new cardiac manifestation associated with woolly hair: report of two cases of woolly hair, palmoplantar keratoderma, and mitral valve regurgitation.
    Zandi S; Farajzadeh S
    Int J Dermatol; 2007 Sep; 46(9):952-4. PubMed ID: 17822500
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Heterogeneity in Waardenburg's syndrome. Report of a family with ocular albinism.
    Bard LA
    Arch Ophthalmol; 1978 Jul; 96(7):1193-8. PubMed ID: 666627
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The ichthyoses.
    Goldsmith LA
    Prog Med Genet; 1976; 1():185-210. PubMed ID: 935508
    [No Abstract]   [Full Text] [Related]  

  • 33. Ichthyosis vulgaris. A clinical and histopathological study of patients and their close relatives in the autosomal dominant and sex-linked forms of the disease.
    Kuokkanen K
    Acta Derm Venereol Suppl (Stockh); 1969; 62():1-72. PubMed ID: 5275917
    [No Abstract]   [Full Text] [Related]  

  • 34. The Okihiro syndrome of Duane anomaly, radial ray abnormalities, and deafness.
    Hayes A; Costa T; Polomeno RC
    Am J Med Genet; 1985 Oct; 22(2):273-80. PubMed ID: 4050857
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Woolly hair nevus: case report and review of literature.
    Gomes TF; Guiote V; Henrique M
    Dermatol Online J; 2020 Jan; 26(1):. PubMed ID: 32155026
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings.
    Froster UG; Rehder H; Höhn W; Oberheuser F
    Am J Med Genet; 1993 Oct; 47(5):717-22. PubMed ID: 8267003
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Repeated epilation (ER): a semidominant autosomal gene reducing synthesis of skin filaggrin in mice.
    Brown KS; Harne LC; Holbrook KA; Dale BA
    Prog Clin Biol Res; 1982; 94():251-64. PubMed ID: 7122618
    [No Abstract]   [Full Text] [Related]  

  • 38. [Trichothiodystrophy: progresssive manifestations].
    Foulc P; Jumbou O; David A; Sarasin A; Stalder JF
    Ann Dermatol Venereol; 1999 Oct; 126(10):703-7. PubMed ID: 10604009
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosis.
    Clayton-Smith J; Donnai D
    J Med Genet; 1989 May; 26(5):339-42. PubMed ID: 2732996
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Biventricular involvement in a Turkish boy with palmoplantar hyperkeratosis and curly hair, an unusual presentation of Naxos-Carvajal syndrome.
    Kilic T; Babaoglu K; Aygün F; Vural A; Ural D; Agacdiken A; Anik Y; Komsuoglu B
    Int J Cardiol; 2007 Feb; 115(3):e122-5. PubMed ID: 17125858
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.