Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 224,326,325 papers from all fields of science
Search
Sign In
Create Free Account
15q24 Microdeletion
Known as:
15q24 Deletion
, 15q24 Microdeletion Syndrome
, Interstitial Deletion of Chromosome 15q24
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
4 relations
Broader (4)
Chromosome Deletion
Chromosomes, Human, Pair 15
Congenital chromosomal disease
Intellectual Disability
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
[Clinical and genetic analysis of three pediatric patients with 15q24 microdeletion syndrome].
X. Jing
,
Lei Zhang
,
+4 authors
C. Liao
Zhonghua yi xue yi chuan xue za zhi = Zhonghua…
2019
Corpus ID: 196614200
OBJECTIVE To explore the genetic basis for three patients with development delay and to correlate their clinical phenotypes with…
Expand
2018
2018
15q24.1 BP4-BP1 microdeletion unmasking paternally inherited functional polymorphisms combined with distal 15q24.2q24.3 duplication in a patient with epilepsy, psychomotor delay, overweight…
Minh-Tuan Huynh
,
A. Lambert
,
+9 authors
A. Receveur
European Journal of Medical Genetics
2018
Corpus ID: 4041863
2017
2017
A Novel Case of 15q24 Microdeletion Syndrome Detected by MLPA in a Chinese Family.
Xiaoying Dai
,
Lu Zhou
,
Yang Liu
,
Jian-sheng Xie
Clinical Laboratory
2017
Corpus ID: 24945580
BACKGROUND Chromosome 15q24 microdeletion syndrome is a rare disease. To date, only 40 cases have been reported. Here, we also…
Expand
2017
2017
[Application of chromosome microarray analysis in 489 children with developmental delay/intellectual disability].
Rongyue Wang
,
T. Lei
,
+6 authors
C. Liao
Zhonghua yi xue yi chuan xue za zhi = Zhonghua…
2017
Corpus ID: 46081845
OBJECTIVE To assess the value of chromosome microarray analysis (CMA) for identifying the etiology of developmental delay…
Expand
Review
2016
Review
2016
An inferential study of the phenotype for the chromosome 15q24 microdeletion syndrome: a bootstrap analysis
A. Palazón-Bru
,
Dolores Ramírez-Prado
,
E. Cortés
,
María Soledad Aguilar-Segura
,
V. Gil-Guillén
PeerJ
2016
Corpus ID: 23239344
In January 2012, a review of the cases of chromosome 15q24 microdeletion syndrome was published. However, this study did not…
Expand
2013
2013
Progressive Dystonia in Mohr‐Tranebjaerg Syndrome With Cochlear Implant and Deep Brain Stimulation
L. Cif
,
Victoria Gonzalez
,
+8 authors
P. Coubes
Movement Disorders
2013
Corpus ID: 206245970
Deafness-dystonia-optic neuronopathy (DDON), or Mohr-Tranebjaerg syndrome (MTS) (Mendelian Inheritance in Man [MIM] no. 304700…
Expand
2010
2010
Corrigendum to: The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype
B. V. Bon
,
D. Koolen
,
+28 authors
B. Vries
European Journal of Human Genetics
2010
Corpus ID: 19936304
Correction to: European Journal of Human Genetics advance online publication 7 October 2009; doi: 10.1038/ejhg.2009.152 Since the…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE