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A boy with dysmorphic features, intellectual disability, and biallelic homozygous deletion in NRXN1.

Holmquist, Peter LU (2015) In Clinical Dysmorphology 24(2). p.75-78
Please use this url to cite or link to this publication:
author
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Clinical Dysmorphology
volume
24
issue
2
pages
75 - 78
publisher
Lippincott Williams & Wilkins
external identifiers
  • pmid:25486015
  • wos:000351266000006
  • scopus:84924985222
ISSN
1473-5717
DOI
10.1097/MCD.0000000000000070
language
English
LU publication?
yes
id
d25fef61-013e-49a7-b34f-6ddbcd134f06 (old id 4908787)
alternative location
http://www.ncbi.nlm.nih.gov/pubmed/25486015?dopt=Abstract
date added to LUP
2015-01-10 13:24:09
date last changed
2017-01-01 03:27:25
@article{d25fef61-013e-49a7-b34f-6ddbcd134f06,
  author       = {Holmquist, Peter},
  issn         = {1473-5717},
  language     = {eng},
  number       = {2},
  pages        = {75--78},
  publisher    = {Lippincott Williams & Wilkins},
  series       = {Clinical Dysmorphology},
  title        = {A boy with dysmorphic features, intellectual disability, and biallelic homozygous deletion in NRXN1.},
  url          = {http://dx.doi.org/10.1097/MCD.0000000000000070},
  volume       = {24},
  year         = {2015},
}