Type II Waardenburg syndrome.
作者信息
Varughese S, Kumar A, Rao S, Puliyel J M
出版信息
Indian Pediatr. 1988 Apr;25(4):384-6.
PMID:3225049
Abstract
摘要
相似文献
1
Type II Waardenburg syndrome.
Indian Pediatr. 1988 Apr;25(4):384-6.
2
[On the Waardenburg syndrome. Case reports].
Otorinolaringol Ital. 1968;36(5):333-47.
3
[Make a diagnosis. Waardenburg's syndrome type 1].
Padiatr Padol. 1983;18(4):399-402.
4
[Waardenburg syndrome].[瓦登伯格综合征]
Orv Hetil. 1977 Aug 28;118(35):2096-9.
5
[Waardenburg syndrome type I--autosomal dominant hereditary combination of multiple facial anomalies with cochlear deafness (author's transl)].Ⅰ型瓦登伯革氏综合征——多种面部异常与耳蜗性耳聋的常染色体显性遗传组合（作者译）
Klin Padiatr. 1982 Mar;194(2):112-6. doi: 10.1055/s-2008-1033785.
6
[Waardenburg's syndrome. A familial case relating to 4 generations and 23 individuals].[瓦登伯革氏综合征。一个涉及四代23人的家族病例]
Ann Genet. 1970 Jun;13(2):125-8.
7
[Waardenburg syndrome. Report of a familial case].[瓦登伯革氏综合征。一例家族性病例报告]
Ann Pediatr (Paris). 1990 Jan;37(1):55-8.
8
Genetic heterogeneity in the Waardenburg syndrome.瓦登伯革氏综合征中的遗传异质性。
Birth Defects Orig Artic Ser. 1971 Mar;07(4):87-101.
9
Inter-oculo-irido-auditory dysplasia. (Waardenburg, van der Hoeve, Halberstsma syndrome).眼间虹膜听觉发育不全。（瓦尔登堡、范德赫夫、哈尔伯茨马综合征）
Bull Ophthalmol Soc Egypt. 1971;64(68):333-7.
10
[A case of Waardenburg-Klein syndrome].[一例瓦登伯格-克莱因综合征病例]
G Ital Dermatol Venereol. 1985 Jul-Aug;120(4):277-9.
Zotero 插件