Spontaneously regressing brain lesions in Smith–Lemli–Opitz syndrome-Reference-Cited by-同舟云学术

Spontaneously regressing brain lesions in Smith–Lemli–Opitz syndrome

Published:2017-12-11 Issue:2 Volume:176 Page:386-390
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Dang Do An N.¹^ORCID,Baker Eva H.²,Warren Katherine E.³,Bianconi Simona E.¹,Porter Forbes D.¹

Affiliation:

1. Division of Translational Research, Eunice Kennedy Shriver National Institute of Human Development (NICHD)National Institutes of Health BethesdaMaryland

2. Department of Radiology and Imaging SciencesClinical CenterNational Institutes of HealthBethesdaMaryland

3. Center for Cancer ResearchNational Cancer InstituteNational Institutes of HealthBethesdaMaryland

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.38563

Reference25 articles.

1. Recent advances in neurofibromatosis type 1

2. Intracranial undifferentiated malign neuroglial tumor in Smith-Lemli-Opitz syndrome: A theory of a possible predisposing factor for primary brain tumors via a case report

3. Female external genitalia and müllerian duct derivatives in a 46,XY infant with the Smith-Lemli-Opitz syndrome

4. Characterizing the microstructural basis of “unidentified bright objects” in neurofibromatosis type 1: A combined in vivo multicomponent T2 relaxation and multi-shell diffusion MRI analysis

5. The smith-lemli-opitz syndrome

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