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Results: 11

Related Articles by Review for PubMed (Select 666627)

1.
2.

Clinical findings in Japanese patients with Waardenburg syndrome type 2.

Ohno N, Kiyosawa M, Mori H, Wang WF, Takase H, Mochizuki M.

Jpn J Ophthalmol. 2003 Jan-Feb;47(1):77-84. Review.

PMID:
12586183
3.

Waardenburg syndrome in Japanese patients. Case reports and literature review.

Hayasaka S, Noda S, Setogawa T, Kobayashi A, Kishida K, Sakai T.

Ophthalmologica. 1992;205(1):46-51. Review.

PMID:
1436991
4.

Heterogeneity in Waardenburg syndrome.

Hageman MJ, Delleman JW.

Am J Hum Genet. 1977 Sep;29(5):468-85. Review.

5.

Hereditary congenital severe deafness syndromes.

Konigsmark BW.

Ann Otol Rhinol Laryngol. 1971 Apr;80(2):269-88. Review. No abstract available.

PMID:
4927796
6.
7.

Waardenburg syndrome type II: phenotypic findings and diagnostic criteria.

Liu XZ, Newton VE, Read AP.

Am J Med Genet. 1995 Jan 2;55(1):95-100. Review.

PMID:
7702105
8.

Waardenburg Syndrome Type I.

Milunsky JM.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015.
2001 Jul 30 [updated 2014 Aug 07].

9.

[CT findings of the temporal bones in Waardenburg's syndrome].

Irie K, Ogata H, Mitsudome A.

No To Hattatsu. 1990 May;22(3):241-6. Review. Japanese.

PMID:
2194542
10.

Hearing impairment and pigmentary disturbance.

Beighton P, Ramesar R, Winship I, Viljoen D, Greenberg J, Young K, Curtis D, Sellars S.

Ann N Y Acad Sci. 1991;630:152-66. Review.

PMID:
1952586
11.
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