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Neurofibromatosis 1 in the setting of dual diagnosis: Diagnostic and management conundrums

  • Published:2021-11-19 Issue: Volume: Page:
  • ISSN:1552-4825
  • Container-title:American Journal of Medical Genetics Part A
  • language:en
  • Short-container-title:Am J Med Genet

Author:

Muthusamy Karthik1ORCID,El‐Jabali Aseel2,Ongie Laura J.1,Dhamija Radhika34,Babovic‐Vuksanovic Dusica156

Affiliation:

1. Department of Clinical Genomics Mayo Clinic Rochester Minnesota USA

2. Alfaisal University Riyadh Saudi Arabia

3. Department of Clinical Genomics Mayo Clinic Phoenix Arizona USA

4. Department of Neurology Mayo Clinic Phoenix Arizona USA

5. Department of Pediatric and Adolescent Medicine Mayo Clinic Rochester Minnesota USA

6. Department of Laboratory Medicine and Pathology Mayo Clinic Rochester Minnesota USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Co-occurrence of neurofibromatosis type 1, caused by Alu insertion, and 16p13.11 microduplication;Egyptian Journal of Medical Human Genetics;2024-09-03

2. Beyond chromosome analysis: Additional genetic testing practice in a Down syndrome clinic;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2023-09-29
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