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 *

201 related articles for article (PubMed ID: 2596512)

  • 21. [A Swiss family with Klein-Waardenburg's syndrome associated with hyperkeratosis of the palms and feet and with serious oligophrenia].
    Amini-Elihou S
    J Genet Hum; 1970 Dec; 18(4):307-63. PubMed ID: 5524816
    [No Abstract]   [Full Text] [Related]  

  • 22. [Chromosome aberrations in the Waardenburg-Klein-Syndrome].
    Partsch CJ; Schleyer KH
    HNO; 1971 Apr; 19(4):121-3. PubMed ID: 5581552
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. [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]  

  • 25. Fluorescence in situ hybridization mapping of 25 markers on distal human chromosome 2q surrounding the human Waardenburg syndrome, type I (WS1) locus (PAX3 gene).
    Lu-Kuo J; Ward DC; Spritz RA
    Genomics; 1993 Apr; 16(1):173-9. PubMed ID: 8486353
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Inter-oculo-irido-auditory dysplasia. (Waardenburg, van der Hoeve, Halberstsma syndrome).
    Mohamed MA
    Bull Ophthalmol Soc Egypt; 1971; 64(68):333-7. PubMed ID: 5005251
    [No Abstract]   [Full Text] [Related]  

  • 27. Prenatal detection of de novo inversion of chromosome (2) (p13q11.2) and postnatal follow-up.
    Kozma C; Subasinghe C; Meck J
    Prenat Diagn; 1996 Apr; 16(4):366-70. PubMed ID: 8734815
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Waardenburg's syndrome and extra chromosome fragment. Study of a family].
    Cordier J; Raspiller A; Gilgenkrantz S
    Bull Mem Soc Fr Ophtalmol; 1972; 85(0):70-81. PubMed ID: 4671855
    [No Abstract]   [Full Text] [Related]  

  • 29. [Waardenburg syndrome].
    Kemény P; Szentesi A; Votisky P; Marczell M
    Orv Hetil; 1977 Aug; 118(35):2096-9. PubMed ID: 909699
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. [Gene responsible for Waardenburg syndrome type I].
    Tsukamoto K; Niikawa N
    Tanpakushitsu Kakusan Koso; 1993 Feb; 38(3):361-5. PubMed ID: 8098159
    [No Abstract]   [Full Text] [Related]  

  • 32. Waardenburg-Hirschsprung disease in two sisters: a possible clue to the genetics of this association?
    Bonnet JP; Till M; Edery P; Attie T; Lyonnet S
    Eur J Pediatr Surg; 1996 Aug; 6(4):245-8. PubMed ID: 8877363
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Recent advances in the understanding of syndromic forms of hearing loss.
    Friedman TB; Schultz JM; Ben-Yosef T; Pryor SP; Lagziel A; Fisher RA; Wilcox ER; Riazuddin S; Ahmed ZM; Belyantseva IA; Griffith AJ
    Ear Hear; 2003 Aug; 24(4):289-302. PubMed ID: 12923420
    [No Abstract]   [Full Text] [Related]  

  • 34. [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]  

  • 35. [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]  

  • 36. [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]  

  • 37. [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]  

  • 38. Autosomal dominant inheritance of Klein-Waardenburg syndrome.
    Sheffer R; Zlotogora J
    Am J Med Genet; 1992 Feb; 42(3):320-2. PubMed ID: 1536170
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. [Waardenburg syndrome with hare-lip and complete palatal cleft].
    Fernández-Lebrez J; López-Rúa RR; Rodríguez Herrera A
    An Esp Pediatr; 1987 Jul; 27(1):77-8. PubMed ID: 3662261
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.