Literature DB >> 4125428

E.M.G. syndrome.

H R Wiedemann.   

Abstract

Mesh：

Year:  1973        PMID： 4125428     DOI： 10.1016/s0140-6736(73)92468-9

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


× No keyword cloud information.
  4 in total

1.  Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome.

Authors:  D Viljoen; R Ramesar
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

2.  Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling.

Authors:  A C Berry; E M Belton; C Chantler
Journal:  J Med Genet       Date:  1980-04       Impact factor: 6.318

3.  Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases.

Authors:  A L Kosseff; J Herrmann; E F Gilbert; C Viseskul; M Lubinsky; J M Opitz
Journal:  Eur J Pediatr       Date:  1976-10-01       Impact factor: 3.183

4.  The Wiedemann-Beckwith syndrome in four sibs including one with associated congenital hypothyroidism.

Authors:  R Martínez y Martínez; R Ocampo-Campos; R Pérez-Arroyo; E Corona-Rivera; J M Cantú
Journal:  Eur J Pediatr       Date:  1985-01       Impact factor: 3.183
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.