Bosley–Salih–Alorainy syndrome in patients from India-Reference-Cited by-同舟云学术

Bosley–Salih–Alorainy syndrome in patients from India

Published:2020-08-31 Issue:11 Volume:182 Page:2699-2703
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Patil Siddaramappa J.¹^ORCID,Karthik Gadabanahalli Ashok²,Bhavani Gandham SriLakshmi³,Bhat Venkatraman²,Matalia Jyoti⁴,Shah Jhanvi¹,Shukla Anju³^ORCID,Girisha Katta Mohan³^ORCID

Affiliation:

1. Division of Medical Genetics, Mazumdar Shaw Medical Center Narayana Hrudayalaya Hospitals Bangalore India

2. Department of Radiology, Mazumdar Shaw Medical Center Narayana Hrudayalaya Hospitals Bangalore India

3. Department of Medical Genetics Kasturba Medical College, Manipal Academy of Higher Education Manipal India

4. Department of Pediatric Ophthalmology & Strabismology Narayana Nethralaya Bangalore India

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61809

Reference15 articles.

1. HOXA1 Mutations are Not Commonly Associated with Non-Syndromic Deafness

2. The clinical spectrum of homozygousHOXA1 mutations

3. Clinical characterization of the HOXA1 syndrome BSAS variant

4. Axons get ahead: Insights into axon guidance and congenital cranial dysinnervation disorders

5. Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism

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