Associated Papers
Bosley-Salih-Alorainy syndrome in patients from India.
Patil SJ et al.
American Journal of Medical Genetics. Part A, 2020
Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss.
Sheppard S et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2018
29907799 (PubMed )
Supplement: 41436_2018_4_MOESM3_ESM.xlsx › variant-_capture___coverage
Human HOX gene disorders.
Quinonez SC et al.
Molecular Genetics and Metabolism, 2014
HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.
Liu J et al.
Pediatric Cardiology, 2013
The clinical spectrum of homozygous HOXA1 mutations.
Bosley TM et al.
American Journal of Medical Genetics. Part A, 2008
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