A boy with dysmorphic features, intellectual disability, and biallelic homozygous deletion in NRXN1.
(2015) In Clinical Dysmorphology 24(2). p.75-78
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/4908787
- author
- Holmquist, Peter LU
- organization
- publishing date
- 2015
- 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
- pmid:25486015
- 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
- 2016-04-01 10:17:55
- date last changed
- 2022-02-17 08:44:06
@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}},
doi = {{10.1097/MCD.0000000000000070}},
volume = {{24}},
year = {{2015}},
}