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 *

88 related articles for article (PubMed ID: 9581391)

  • 21. The Waardenburg syndrome.
    Pantke OA; Cohen MM
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):147-52. PubMed ID: 5173203
    [No Abstract]   [Full Text] [Related]  

  • 22. The eyes have it: Waardenburg's syndrome.
    Enright KA; Neelon FA
    N C Med J; 1986 Dec; 47(12):592-6. PubMed ID: 3468364
    [No Abstract]   [Full Text] [Related]  

  • 23. [Waardenburg's syndrome in the newborn infant. Report of a case].
    Senigagliesi L; Pierro U; Paradiso M
    Minerva Pediatr; 1977 Apr; 29(13):967-70. PubMed ID: 875976
    [No Abstract]   [Full Text] [Related]  

  • 24. [A new case of Waardenburg's syndrome].
    Malbrel C; Longuebray P; Jouhaud F
    Bull Soc Ophtalmol Fr; 1982 Apr; 82(4):579-81. PubMed ID: 7105357
    [No Abstract]   [Full Text] [Related]  

  • 25. [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]  

  • 26. [Waardenburg-Klein syndrome. Description of 2 cases].
    Fregonese B; Vignola G; Mori PG; Grossi Bianchi ML
    Minerva Pediatr; 1969 Aug; 21(33):1513-9. PubMed ID: 5361984
    [No Abstract]   [Full Text] [Related]  

  • 27. Waardenburg syndrome type 1.
    Karaman A; Aliagaoglu C
    Dermatol Online J; 2006 Mar; 12(3):21. PubMed ID: 16638435
    [TBL] [Abstract][Full Text] [Related]  

  • 28. An unusual eye-ear syndrome with renal abnormality.
    Murdoch JL; Mengel MC
    Birth Defects Orig Artic Ser; 1971 Mar; 07(4):136. PubMed ID: 5006207
    [No Abstract]   [Full Text] [Related]  

  • 29. Symposium on sensorineural hearing loss in children: early detection and intervention. Evaluation of the child with sensorineural hearing impairment.
    Linthicum FH
    Otolaryngol Clin North Am; 1975 Feb; 8(1):69-75. PubMed ID: 1167956
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Waardenburg syndrome associated with laryngomalacia.
    Thapa R; Mallick D; Ghosh A; Ghosh A
    Singapore Med J; 2009 Dec; 50(12):e401-3. PubMed ID: 20087539
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Phenotypic discriminants in the Waardenburg syndrome.
    Winship I; Beighton P
    Clin Genet; 1992 Apr; 41(4):181-8. PubMed ID: 1576755
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Waardenburg's syndrome.
    Joseph TA; Chakravarthy KS
    Indian J Ophthalmol; 1980 Apr; 28(1):37-8. PubMed ID: 7203595
    [No Abstract]   [Full Text] [Related]  

  • 33. Waardenburg syndrome with extended aganglionosis: report of 3 new cases.
    Karaca I; Turk E; Ortac R; Kandirici A
    J Pediatr Surg; 2009 Jun; 44(6):E9-13. PubMed ID: 19524716
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Waardenburg Syndrome: a review of literature and case reports].
    Salvatore S; Carnevale C; Infussi R; Arrico L; Mafrici M; Plateroti AM; Vingolo EM
    Clin Ter; 2012; 163(2):e85-94. PubMed ID: 22555841
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Association of Shah-Waardenburgh syndrome: a review of 6 cases.
    Jan IA; Stroedter L; Haq AU; Din ZU
    J Pediatr Surg; 2008 Apr; 43(4):744-7. PubMed ID: 18405726
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Main symptom: congenital bilateral facial paralysis].
    Kretschmer H
    Klin Monbl Augenheilkd; 1969 May; 154(5):733-8. PubMed ID: 5352393
    [No Abstract]   [Full Text] [Related]  

  • 38. Anophthalmos with limb anomalies (Waardenburg opththalmo-acromelic syndrome): report of a new Italian case with renal anomaly and review.
    Garavelli L; Pedori S; Dal Zotto R; Franchi F; Marinelli M; Croci GF; Bellato S; Ammenti A; Virdis R; Banchini G; Superti-Furga A
    Genet Couns; 2006; 17(4):449-55. PubMed ID: 17375532
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Atypical manifestations in familial type 1 Waardenburg syndrome].
    Sans B; Calvas P; Bazex J
    Ann Dermatol Venereol; 1998 Jan; 125(1):37-41. PubMed ID: 9747206
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Recognition and diagnosis of hereditary deafness with tomographic correlations.
    Marcus RE
    Trans Am Acad Ophthalmol Otolaryngol; 1969; 73(3):409-19. PubMed ID: 5791364
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.