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 *

140 related articles for article (PubMed ID: 7098370)

  • 1. [Waardenburg syndrome type I--autosomal dominant hereditary combination of multiple facial anomalies with cochlear deafness (author's transl)].
    Meinecke P
    Klin Padiatr; 1982 Mar; 194(2):112-6. PubMed ID: 7098370
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Waardenburg syndrome. Report of a familial case].
    Khaldi F; Serbegi M; Mokadem H; Lazzem B; Bennaceur B
    Ann Pediatr (Paris); 1990 Jan; 37(1):55-8. PubMed ID: 2316963
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Waardenburg's syndrome. A familial case relating to 4 generations and 23 individuals].
    Roux C; Baheux G; Gaulier M; Caldera R; Soepardan L
    Ann Genet; 1970 Jun; 13(2):125-8. PubMed ID: 5310696
    [No Abstract]   [Full Text] [Related]  

  • 4. Type II Waardenburg syndrome.
    Varughese S; Kumar A; Rao S; Puliyel JM
    Indian Pediatr; 1988 Apr; 25(4):384-6. PubMed ID: 3225049
    [No Abstract]   [Full Text] [Related]  

  • 5. Waardenburg syndrome type II: phenotypic findings and diagnostic criteria.
    Liu XZ; Newton VE; Read AP
    Am J Med Genet; 1995 Jan; 55(1):95-100. PubMed ID: 7702105
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A case of Waardenburg-Klein syndrome observed at the Cotonou NUHC].
    Bassabi SK; Medji AP; Doutetien C; Oussa G; Hounkpe YY; Vodouhe SJ; Babagbeto M; Latoundji S
    J Fr Ophtalmol; 1997; 20(5):387-90. PubMed ID: 9238477
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Waardenburg's syndrome in Kenyan Africans.
    Hageman MJ
    Trop Geogr Med; 1978 Mar; 30(1):45-55. PubMed ID: 675827
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Waardenburg syndrome: a report of three cases.
    Ghosh SK; Bandyopadhyay D; Ghosh A; Biswas SK; Mandal RK
    Indian J Dermatol Venereol Leprol; 2010; 76(5):550-2. PubMed ID: 20826997
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic heterogeneity in the Waardenburg syndrome.
    Arias S
    Birth Defects Orig Artic Ser; 1971 Mar; 07(4):87-101. PubMed ID: 5006208
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Klein-Waardenburg syndrome. Report of 3 cases in a family with a review of the literature].
    Piechowiak H; Wasmer C; Göbel FD
    Laryngol Rhinol Otol (Stuttg); 1985 Apr; 64(4):194-7. PubMed ID: 4010406
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Make a diagnosis. Waardenburg's syndrome type 1].
    Aksu F
    Padiatr Padol; 1983; 18(4):399-402. PubMed ID: 6646790
    [No Abstract]   [Full Text] [Related]  

  • 12. [Waardenburg's syndrome. Clinical and genetical study of a family with affected twins].
    Carakushansky G; Berthier C
    AMB Rev Assoc Med Bras; 1975 May; 21(5):159-60. PubMed ID: 1088764
    [No Abstract]   [Full Text] [Related]  

  • 13. Waardenburg syndrome--penetrance of major signs.
    Preus M; Linstrom C; Polomeno RC; Milot J
    Am J Med Genet; 1983 Jul; 15(3):383-8. PubMed ID: 6881207
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [On the Waardenburg syndrome. Case reports].
    Bernabei L; Pierangeli CE; Di Brino M; Baldiserri L
    Otorinolaringol Ital; 1968; 36(5):333-47. PubMed ID: 5703882
    [No Abstract]   [Full Text] [Related]  

  • 15. Mental retardation and EEG abnormalities in Waardenburg's syndrome: two case reports (EEG anomalies in Waardenburg's syndrome).
    Cantani A; Bamonte G; Tacconi ML
    Padiatr Padol; 1989; 24(2):137-40. PubMed ID: 2503803
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Waardenburg syndrome in the Turkish deaf population.
    Silan F; Zafer C; Onder I
    Genet Couns; 2006; 17(1):41-8. PubMed ID: 16719276
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Waardenburg's syndrome. Report of a family (author's transl)].
    Gracia R; Burgueros M; Lledó G; Barrio R; Alvarado F
    An Esp Pediatr; 1975; 8(4):429-34. PubMed ID: 1147417
    [No Abstract]   [Full Text] [Related]  

  • 18. Brief clinical report: autosomal recessive anophthalmia with multiple congenital abnormalities--type Waardenburg.
    Richieri-Costa A; Gollop TR; Otto PG
    Am J Med Genet; 1983 Apr; 14(4):607-15. PubMed ID: 6846395
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndrome.
    Stoll C; Terzic J; Fischbach M
    Genet Couns; 1999; 10(4):337-43. PubMed ID: 10631920
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Hereditary unilateral deaf-mutism as a variable manifestation of bilateral deaf-mutism or hearing loss].
    Graf K
    Laryngorhinootologie; 1992 May; 71(5):242-5. PubMed ID: 1616543
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.