Eruptive keratotic melanocytic nevi in 2p deletion syndrome
Author:
Affiliation:
1. Dermatology South Infirmary Victoria University Hospital Cork Ireland
2. INFANT Research Centre University College Cork Cork Ireland
Publisher
Wiley
Subject
Dermatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijd.16943
Reference5 articles.
1. Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1
2. De novo deletion (2) (p11.2p13): clinical, cytogenetic, and immunological data.
3. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders
4. Rare Chromosome Disorder Support Group (Internet). 2p16.3 (NRXN1) deletions. Surrey (UK).2014. Accessed May 10 2023.https://www.rarechromo.org/media/information/Chromosome%20%202/2p16.3%20(NRXN1)%20deletions%20FTNW.pdf
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