[Wiedemann and Beckwith syndrome: a new familial case].
作者信息
Piussan C, Risbourg B, Lenaerts C, Delvallez N, Gontier M F, Vitse M
出版信息
J Genet Hum. 1980 Sep;28(3):281-91.
PMID:7463028
Abstract
摘要
相似文献
1
[Wiedemann and Beckwith syndrome: a new familial case].[维德曼和贝克威思综合征：一例新的家族性病例]
J Genet Hum. 1980 Sep;28(3):281-91.
2
Familial occurrence of the Wiedemann-Beckwith syndrome and persistent fontanel.威德曼-贝克威思综合征和囟门持续未闭的家族性发病情况。
Am J Med Genet. 1977;1(1):59-63. doi: 10.1002/ajmg.1320010107.
3
[The Beckwith-Wiedemann syndrome. Six observations with three familial forms (author's transl)].[贝克威思-维德曼综合征。三例家族性病例及六例观察报告（作者译）]
Ann Pediatr (Paris). 1981 Nov;28(9):665-70.
4
[Wiedemann-Beckwith syndrome. Study of an oligosymptomatic form].[威德曼-贝克威思综合征。一种轻症形式的研究]
Monatsschr Kinderheilkd. 1986 Aug;134(8):554-7.
5
Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family.威德曼-贝克威思综合征：一个家族中的常染色体显性遗传。
Am J Med Genet. 1981;9(4):291-9. doi: 10.1002/ajmg.1320090405.
6
[Family with Wiedemann-Beckwith syndrome].[患有威德曼-贝克威思综合征的家族]
Horumon To Rinsho. 1975 Jun;23(6):626-30.
7
[Beckwith-Wiedemann syndrome with pancreatic fibro-adenosis (author's transl)].伴有胰腺纤维腺瘤的贝克威思-维德曼综合征（作者译）
Arch Anat Cytol Pathol. 1981;29(5):273-8.
8
Macroglossia in the Beckwith-Wiedemann syndrome.
Trans Sect Otolaryngol Am Acad Ophthalmol Otolaryngol. 1977 Jan-Feb;84(1):116-9.
9
[EMG syndrome. Review apropo of 2 cases].[肌电图综合征。关于2例病例的综述]
Med Cutan Ibero Lat Am. 1977;5(1):53-8.
10
[Wiedemann-Beckwith syndrome (omphalocele-macroglossia-gigantism)].
Ann Pediatr (Paris). 1969 Jan 2;16(1):49-56.
引用本文的文献
1
Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature.维德曼-贝克威思综合征：22例新病例的临床和细胞遗传学数据展示及文献综述
Hum Genet. 1986 Oct;74(2):143-54. doi: 10.1007/BF00282078.
2
Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome.贝克威思-维德曼综合征患者胰岛素及胰岛素样生长因子II基因的正常剂量
Am J Hum Genet. 1986 Aug;39(2):265-73.
3
Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome.家族性贝克威思-维德曼综合征中父系印记的证据。
J Med Genet. 1992 Apr;29(4):221-5. doi: 10.1136/jmg.29.4.221.
Zotero 插件