Prenatal ultrasound and MRI findings of temporal and occipital lobe dysplasia in a twin with achondroplasia-Reference-Cited by-同舟云学术

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Prenatal ultrasound and MRI findings of temporal and occipital lobe dysplasia in a twin with achondroplasia

Published:2014-08-25 Issue:3 Volume:44 Page:365-368
ISSN:0960-7692
Container-title:Ultrasound in Obstetrics & Gynecology
language:en
Short-container-title:Ultrasound Obstet Gynecol

Author:

Pugash D.¹,Lehman A. M.²,Langlois S.²

Affiliation:

1. Department of Radiology; British Columbia Women's Hospital and University of British Columbia; Vancouver Canada

2. Department of Medical Genetics; British Columbia Women's Hospital and University of British Columbia; Vancouver Canada

Publisher

Wiley

Subject

Obstetrics and Gynaecology,Radiology Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology

Reference15 articles.

1. FGFR3 mutations and medial temporal lobe dysgenesis;Kannu;J Child Neurol,2007

2. Neuroimaging and neurological findings in patients with hypochondroplasia and FGFR3 N540K mutation;Linnankivi;Am J Med Genet A,2012

3. Temporal and occipital lobe features in children with hypochondroplasia/FGFR3 gene mutation;Philpott;Pediatr Radiol,2013

4. A common FGFR3 gene mutation in hypochondroplasia;Prinos;Hum Mol Genet,1995

5. Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data;Tsai;Am J Med Genet,1999

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