Microdeletion Syndromes
Author:
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/9780470015902.a0005549.pub2
Reference56 articles.
1. The face of Smith–Magenis syndrome: a subjective and objective study;Allanson JE;Journal of Medical Genetics,1999
2. Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designs
3. Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome
4. High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions
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1. Invivo and systematic analysis of random multigenic deletions associated with human diseases during epithelial morphogenesis in Drosophila;2021-01-21
2. Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations;Journal of Neurodevelopmental Disorders;2018-08-29
3. Prenatal Diagnosis Innovation: Genome Sequencing of Maternal Plasma;Annual Review of Medicine;2016-01-14
4. Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening;European Journal of Human Genetics;2015-03-18
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