Expanding the clinico‐molecular spectrum of Angelman syndrome phenotype with the GABRG3 gene: Evidence from methylation and sequencing studies-Reference-Cited by-同舟云学术

Expanding the clinico‐molecular spectrum of Angelman syndrome phenotype with the GABRG3 gene: Evidence from methylation and sequencing studies

Author:

Iyer Gayatri R.¹²,Utage Prashant³⁴,Devi Radha Rama⁵,Vattam Kiran Kumar⁶⁷,Hasan Qurratulain¹

Affiliation:

1. Department of Genetics & Molecular Medicine Kamineni Hospitals Hyderabad Telangana India

2. Department of Genetics Osmania University Hyderabad Telangana India

3. Department of Pediatrics Kamineni Hospitals Hyderabad Telangana India

4. Department of Pediatric Neurology Utage Child Development Center Hyderabad Telangana India

5. Department of Pediatrics ‐ Rainbow Hospitals Hyderabad Telangana India

6. Department of Genomics & Molecular Diagnostics, Sandor Specialty Diagnostics Hyderabad Telangana India

7. Department of Cytogenetics, Sandor Speciality Diagnostics Hyderabad Telangana India

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference22 articles.

1. Angelman syndrome: Review of clinical and molecular aspects;Bird L;The Application of Clinical Genetics

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