Chromosome 15 Imprinting Disorders: Genetic Laboratory Methodology and Approaches
Published 2020 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Chromosome 15 Imprinting Disorders: Genetic Laboratory Methodology and Approaches
Authors
Keywords
-
Journal
Frontiers in Pediatrics
Volume 8, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2020-05-12
DOI
10.3389/fped.2020.00154
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Prader–Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion
- (2020) Qiming Tan et al. Genes
- Analysis of the Prader-Willi syndrome imprinting center using droplet digital PCR and next-generation whole-exome sequencing
- (2019) Samantha N. Hartin et al. Molecular Genetics & Genomic Medicine
- Preserved expressive language as a phenotypic determinant of Mosaic Angelman Syndrome
- (2019) Robert P. Carson et al. Molecular Genetics & Genomic Medicine
- An overview of health issues and development in a large clinical cohort of children with Angelman syndrome
- (2019) Karen G. C. B. Bindels‐de Heus et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Multi-Method Assessment of Sleep in Children With Angelman Syndrome: A Case–Controlled Study
- (2019) Jayne Trickett et al. Frontiers in Psychiatry
- Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review
- (2018) Samantha N. Hartin et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study
- (2018) Merlin G Butler et al. JOURNAL OF MEDICAL GENETICS
- Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects
- (2016) Maaz Hassan et al. European Journal of Medical Genetics
- Angelman syndrome — insights into a rare neurogenetic disorder
- (2016) Karin Buiting et al. Nature Reviews Neurology
- Angelman Syndrome
- (2015) Seth S. Margolis et al. Neurotherapeutics
- Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings
- (2015) M. A. Angulo et al. JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
- Clinical utility gene card for: Angelman Syndrome
- (2014) Karin Buiting et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Prader-Willi syndrome
- (2012) Suzanne B. Cassidy et al. GENETICS IN MEDICINE
- Nutritional phases in Prader-Willi syndrome
- (2011) Jennifer L. Miller et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Behavior and neuropsychiatric manifestations in Angelman syndrome
- (2011) Bernard Dan Neuropsychiatric Disease and Treatment
- Clinical and genetic aspects of Angelman syndrome
- (2010) Charles A Williams et al. GENETICS IN MEDICINE
- Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster
- (2008) Trilochan Sahoo et al. NATURE GENETICS
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now