87 related articles for article (PubMed ID: 1303254)
1. Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1.
Steel KP; Smith RJ
Nat Genet; 1992 Sep; 2(1):75-9. PubMed ID: 1303254
[TBL] [Abstract][Full Text] [Related]
2. A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1.
Hughes AE; Newton VE; Liu XZ; Read AP
Nat Genet; 1994 Aug; 7(4):509-12. PubMed ID: 7951321
[TBL] [Abstract][Full Text] [Related]
3. [Waardenburg's syndrome].
Cacheux V; Delezoide AL; Vekemans M
C R Seances Soc Biol Fil; 1996; 190(5-6):577-80. PubMed ID: 9074723
[TBL] [Abstract][Full Text] [Related]
4. Finding the gene(s) for Waardenburg syndrome(s).
Grundfast KM; San Agustin TB
Otolaryngol Clin North Am; 1992 Oct; 25(5):935-51. PubMed ID: 1408197
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene.
Tassabehji M; Newton VE; Read AP
Nat Genet; 1994 Nov; 8(3):251-5. PubMed ID: 7874167
[TBL] [Abstract][Full Text] [Related]
7. Waardenburg I syndrome: a clinical and genetic study of two large Brazilian kindreds, and literature review.
da-Silva EO
Am J Med Genet; 1991 Jul; 40(1):65-74. PubMed ID: 1887852
[TBL] [Abstract][Full Text] [Related]
8. Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome).
Amiel J; Watkin PM; Tassabehji M; Read AP; Winter RM
Clin Dysmorphol; 1998 Jan; 7(1):17-20. PubMed ID: 9546825
[TBL] [Abstract][Full Text] [Related]
9. Pax and vertebrate development.
Wehr R; Gruss P
Int J Dev Biol; 1996 Feb; 40(1):369-77. PubMed ID: 8735950
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. SOX10 mutations in patients with Waardenburg-Hirschsprung disease.
Pingault V; Bondurand N; Kuhlbrodt K; Goerich DE; Préhu MO; Puliti A; Herbarth B; Hermans-Borgmeyer I; Legius E; Matthijs G; Amiel J; Lyonnet S; Ceccherini I; Romeo G; Smith JC; Read AP; Wegner M; Goossens M
Nat Genet; 1998 Feb; 18(2):171-3. PubMed ID: 9462749
[TBL] [Abstract][Full Text] [Related]
12. Animal models of pigment and hearing abnormalities in man.
Brown KS; Bergsma DR; Barrow MV
Birth Defects Orig Artic Ser; 1971 Mar; 07(4):102-9. PubMed ID: 5173333
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [Waardenburg's syndrome (type II) in 2 children, without parental involvement: genetic counseling].
Dodinval P; Lhussier-Grodos TM
J Genet Hum; 1981 Sep; 29(3):273-84. PubMed ID: 7334349
[No Abstract] [Full Text] [Related]
15. Analysis of SOX10 mutations identified in Waardenburg-Hirschsprung patients: Differential effects on target gene regulation.
Chan KK; Wong CK; Lui VC; Tam PK; Sham MH
J Cell Biochem; 2003 Oct; 90(3):573-85. PubMed ID: 14523991
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Molecular heterogeneity in two families with auditory pigmentary syndromes: the role of neuroimaging and genetic analysis in deafness.
Shears D; Conlon H; Murakami T; Fukai K; Alles R; Trembath R; Bitner-Glindzicz M
Clin Genet; 2004 May; 65(5):384-9. PubMed ID: 15099345
[TBL] [Abstract][Full Text] [Related]
18. Point mutation in the MITF gene causing Waardenburg syndrome type II in a three-generation Indian family.
Lalwani AK; Attaie A; Randolph FT; Deshmukh D; Wang C; Mhatre A; Wilcox E
Am J Med Genet; 1998 Dec; 80(4):406-9. PubMed ID: 9856573
[TBL] [Abstract][Full Text] [Related]
19. Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3).
Ishikiriyama S; Tonoki H; Shibuya Y; Chin S; Harada N; Abe K; Niikawa N
Am J Med Genet; 1989 Aug; 33(4):505-7. PubMed ID: 2596512
[TBL] [Abstract][Full Text] [Related]
20. [New observation of the severe form of the Klein-Waardenburg syndrome].
Wilbrandt HR; Ammann F
Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg; 1964; 39(1-4):80-92. PubMed ID: 5899973
[No Abstract] [Full Text] [Related]
[Next] [New Search]
