Literature DB >> 20354438

KBG syndrome associated with periventricular nodular heterotopia.

Renske Oegema1, Rachel Schot, Marie Claire Y de Wit, Maarten H Lequin, Rianne Oostenbrink, Irenaeus F M de Coo, Grazia M S Mancini.   

Abstract

Entities:  

Mesh：

Year:  2010        PMID： 20354438     DOI： 10.1097/MCD.0b013e3283387b3b

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


× No keyword cloud information.
  3 in total

1.  Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations.

Authors:  Charlotte W Ockeloen; Marjolein H Willemsen; Sonja de Munnik; Bregje W M van Bon; Nicole de Leeuw; Aad Verrips; Sarina G Kant; Elizabeth A Jones; Han G Brunner; Rosa L E van Loon; Eric E J Smeets; Mieke M van Haelst; Gijs van Haaften; Ann Nordgren; Helena Malmgren; Giedre Grigelioniene; Sascha Vermeer; Pedro Louro; Lina Ramos; Thomas J J Maal; Celeste C van Heumen; Helger G Yntema; Carine E L Carels; Tjitske Kleefstra
Journal:  Eur J Hum Genet       Date:  2014-11-26       Impact factor: 4.246

2.  Intellectual Profiles in KBG-Syndrome: A Wechsler Based Case-Control Study.

Authors:  Linde C M van Dongen; Ellen Wingbermühle; Wouter Oomens; Anja G Bos-Roubos; Charlotte W Ockeloen; Tjitske Kleefstra; Jos I M Egger
Journal:  Front Behav Neurosci       Date:  2017-12-19       Impact factor: 3.558

Review 3.  KBG syndrome.

Authors:  Dayna Morel Swols; Joseph Foster; Mustafa Tekin
Journal:  Orphanet J Rare Dis       Date:  2017-12-19       Impact factor: 4.123
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.