Skip to content
Open Access
  • Home
  • Collections
    • High Impact Articles
    • Jawi Collection
    • Malay Medicine
    • Forensic
  • Search Options
    • UiTM Open Access
    • Search by UiTM Scopus
    • Advanced Search
    • Search by Category
  • Discovery Service
    • Sources
    • UiTM Journals
    • List UiTM Journal in IR
    • Statistic
  • About
    • Open Access
    • Creative Commons Licenses
    • COKI | Malaysia Open Access
    • User Guide
    • Contact Us
    • Search Tips
    • FAQs
Advanced
  • Search
  • Short stature and microcephaly...
  • Cite this
  • Text this
  • Email this
  • Print
  • Export Record
    • Export to RefWorks
    • Export to EndNoteWeb
    • Export to EndNote
  • Permanent link
Short stature and microcephaly in two siblings due to a novel de novo IGF1R variant

Short stature and microcephaly in two siblings due to a novel de novo IGF1R variant

Bibliographic Details
Main Authors: Alexandra Gkourogianni, Ingrid Alvarez, Sigrun Hallgrimsdottir, Anna Ek, Ola Nilsson
Format: Article
Language:English
Published: Elsevier 2020-10-01
Series:Bone Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2352187220302606
  • Holdings
  • Description
  • Similar Items
  • Staff View

Internet

http://www.sciencedirect.com/science/article/pii/S2352187220302606

Similar Items

  • Short Stature Homeobox-Containing Haploinsufficiency in Seven Siblings with Short Stature
    by: Elizabeth S. Sandberg, et al.
    Published: (2017-01-01)
  • Serum IGF-1 and short stature in adolescents with beta-thalassemia major
    by: Monalisa Elizabeth, et al.
    Published: (2018-07-01)
  • Short stature and SHOX (Short stature homeobox) variants—efficacy of screening using various strategies
    by: Pavlina Capkova, et al.
    Published: (2020-11-01)
  • The recommended starting dose of 0.4mg/kg burosumab is insufficient for most children with X-linked hypophosphatemia (XLH) - Results from the first treated patients in Sweden
    by: Sigrun Hallgrimsdottir, et al.
    Published: (2020-10-01)
  • Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings.
    by: Charlotte Mouden, et al.
    Published: (2015-01-01)

© 2020 | Services hosted by the Perpustakaan Tun Abdul Razak, | Universiti Teknologi MARA | Disclaimer


Loading...