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Waardenburg's syndrome. Report of a family.

作者信息

Cant J S, Martin A J

出版信息

Br J Ophthalmol. 1967 Nov;51(11):755-9. doi: 10.1136/bjo.51.11.755.

DOI:10.1136/bjo.51.11.755
PMID:6060805
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC506489/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82fa/506489/d786b3ae7456/brjopthal00359-0038-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82fa/506489/f40cd3cb9f88/brjopthal00359-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82fa/506489/d786b3ae7456/brjopthal00359-0038-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82fa/506489/f40cd3cb9f88/brjopthal00359-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82fa/506489/d786b3ae7456/brjopthal00359-0038-a.jpg

相似文献

1
Waardenburg's syndrome. Report of a family.瓦登伯革氏综合征。一个家族的报告。
Br J Ophthalmol. 1967 Nov;51(11):755-9. doi: 10.1136/bjo.51.11.755.
2
[Waardenburg's syndrome in three generations of one family].
Nihon Ganka Kiyo. 1966 Feb;17(2):150-3.
3
A Chinese family with Waardenburg's syndrome.
Am J Ophthalmol. 1968 Feb;65(2):174-82.
4
Waardenburg's syndrome during the first year of life.
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5
Tomography of the inner ear in a case of Waardenburg's syndrome.瓦登伯格综合征一例的内耳体层摄影术
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6
[Waardenburg's syndrome. (Apropos of a familial case)].
Rev Otoneuroophtalmol. 1966 Mar-Apr;38(2):89-91.
7
[Waardenburg's syndrome demonstrated on 5 families].
Z Kinderheilkd. 1965 Sep 3;93(4):295-313.
8
[New observation of the severe form of the Klein-Waardenburg syndrome].
Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg. 1964;39(1-4):80-92.
9
Pigmentary disorders in association with congenital deafness.伴有先天性耳聋的色素沉着障碍。
Arch Dermatol. 1967 Feb;95(2):176-86.
10
The Waardenburg syndrome. Description and report of a search.瓦登伯革氏综合征。描述及一项检索报告。
Clin Pediatr (Phila). 1965 Dec;4(12):739-44. doi: 10.1177/000992286500401210.

引用本文的文献

1
Waardenburg's memorial lecture: Waardenburg's syndrome.
Int Ophthalmol. 1982 May;5(1):3-13. doi: 10.1007/BF00129991.
2
Waardenburg's syndrome. Report of a case with family studies.
Indian J Pediatr. 1969 Dec;36(263):483-5. doi: 10.1007/BF02821375.
3
Heterogeneity in Waardenburg syndrome.瓦登伯革氏综合征的异质性。
Am J Hum Genet. 1977 Sep;29(5):468-85.

本文引用的文献

1
WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION.聋校学生中的瓦登伯革氏综合征与虹膜异色症
Can Med Assoc J. 1964 Apr 25;90(17):1008-17.
2
Waardenburg's syndrome.
Acta Ophthalmol (Copenh). 1962;40:622-8. doi: 10.1111/j.1755-3768.1962.tb07838.x.
3
Waardenburg's syndrome in father and daughter.
Acta Ophthalmol (Copenh). 1962;40:590-9. doi: 10.1111/j.1755-3768.1962.tb07835.x.
4
Deafness as part of an hereditary syndrome.
作为遗传性综合征一部分的耳聋。
J Laryngol Otol. 1959 Jun;73:355-82. doi: 10.1017/s0022215100055420.
5
Waardenburg's syndrome. A syndrome of heterochromia of the iridies, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects.瓦登伯格综合征。一种具有虹膜异色、内眦和泪点外侧移位、先天性耳聋以及其他相关特征性缺陷的综合征。
Trans Am Acad Ophthalmol Otolaryngol. 1960 Nov-Dec;64:816-39.