159 related articles for article (PubMed ID: 6651333)
21. Waardenburg's syndrome: variations in expressivity.
Wang L; Karmody CS; Pashayan H
Otolaryngol Head Neck Surg; 1981; 89(4):666-70. PubMed ID: 6793979
[TBL] [Abstract][Full Text] [Related]
22. Defect of neutrophil mobility with dominant inheritance in a family with Waardenburg's syndrome.
Super M
Arch Dis Child; 1981 Oct; 56(10):814. PubMed ID: 7305423
[No Abstract] [Full Text] [Related]
23. Waardenburg's syndrome.
Arias S
J Med Genet; 1980 Jun; 17(3):243. PubMed ID: 7401140
[No Abstract] [Full Text] [Related]
24. Waardenburg syndrome.
De Laey JJ; Meire F; Standaert L; Zeng LH
Yan Ke Xue Bao; 1987 Mar; 3(1):10-5. PubMed ID: 3149590
[No Abstract] [Full Text] [Related]
25. Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene.
Badner JA; Chakravarti A
Am J Med Genet; 1990 Jan; 35(1):100-4. PubMed ID: 2301458
[TBL] [Abstract][Full Text] [Related]
26. [Waardenburg's syndrome. Four cases in an Iranian family (author's transl)].
Walizadeh GR; Kabiri M
Monatsschr Kinderheilkd (1902); 1978 Apr; 126(4):212-4. PubMed ID: 651897
[TBL] [Abstract][Full Text] [Related]
27. Waardenburg syndrome associated with Hirschsprung disease and other abnormalities.
de Lumley Woodyear L; Boulesteix J; Rutkowski J; Umdenstock R
Pediatrics; 1980 Feb; 65(2):368-9. PubMed ID: 7354993
[No Abstract] [Full Text] [Related]
28. Intestinal aganglionosis associated with the Waardenburg syndrome: report of two cases and review of the literature.
Toki F; Suzuki N; Inoue K; Suzuki M; Hirakata K; Nagai K; Kuroiwa M; Lupski JR; Tsuchida Y
Pediatr Surg Int; 2003 Dec; 19(11):725-8. PubMed ID: 14691634
[TBL] [Abstract][Full Text] [Related]
29. Waardenburg's syndrome: the need for family investigation and genetic counselling.
Parving A; Mogensen C
Scand Audiol; 1981; 10(2):121-3. PubMed ID: 7280541
[No Abstract] [Full Text] [Related]
30. Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease.
Attié T; Till M; Pelet A; Amiel J; Edery P; Boutrand L; Munnich A; Lyonnet S
Hum Mol Genet; 1995 Dec; 4(12):2407-9. PubMed ID: 8634719
[No Abstract] [Full Text] [Related]
31. Pigment distribution in Waardenburg's syndrome: a new hypothesis.
Nork TM; Shihab ZM; Young RS; Price J
Graefes Arch Clin Exp Ophthalmol; 1986; 224(6):487-92. PubMed ID: 3792843
[TBL] [Abstract][Full Text] [Related]
32. Waardenburg's syndrome and familial periodic paralysis.
Tay CH
Postgrad Med J; 1971 Jun; 47(548):354-60. PubMed ID: 5580938
[TBL] [Abstract][Full Text] [Related]
33. Partial anodontia in a case of Waardenburg's syndrome.
Bandyopadhyay S; Prasad S; Singhania PK
J Laryngol Otol; 1999 Jul; 113(7):672-4. PubMed ID: 10605569
[TBL] [Abstract][Full Text] [Related]
34. White forelock, pigmentary disorder of irides, and long segment Hirschsprung disease: possible variant of Waardenburg syndrome.
Shah KN; Dalal SJ; Desai MP; Sheth PN; Joshi NC; Ambani LM
J Pediatr; 1981 Sep; 99(3):432-5. PubMed ID: 7264803
[No Abstract] [Full Text] [Related]
35. [Waardenburg's syndrome associated with a generalized epileptic seizure. Cerebral tomodensitometric study].
Sanyas P; Cotineau J; Rudler J
Sem Hop; 1982 Oct; 58(38):2215-7. PubMed ID: 6294866
[TBL] [Abstract][Full Text] [Related]
36. Shah-Waardenburg syndrome.
Sankar R
Dermatol Online J; 2008 Jan; 14(1):19. PubMed ID: 18319036
[TBL] [Abstract][Full Text] [Related]
37. Waardenburg's syndrome in two siblings, both parents and their maternal grandmother.
David TJ; Warin RP
Proc R Soc Med; 1972 Jul; 65(7):601-2. PubMed ID: 5085935
[No Abstract] [Full Text] [Related]
38. Genetic characterization of a patient with an unusual presentation of Waardenburg syndrome Type 4 and retinoblastoma.
Shanthini T; Balaji S; Kim U; Muthukkaruppan V; Vanniarajan A
Pediatr Blood Cancer; 2021 Jan; 68(1):e28553. PubMed ID: 32672397
[No Abstract] [Full Text] [Related]
39. 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]
40. A coloured family showing features of Waardenburg's syndrome.
Rappoport AS
S Afr Med J; 1970 Apr; 44(14):412-3. PubMed ID: 5443890
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
