Showing results 1 to 5 of 5
| Title | Author(s) | Issue Date | Views | |
|---|---|---|---|---|
| 2014 | 77 | |||
CFTR: I1023R is a rare but recurrent disease-causing mutation found in Chinese patients with cystic fibrosis Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2014 | 2014 | 87 | ||
Expanded Prader-Willi Syndrome Due to Chromosome 15q11.2-14 Deletion: Report and a Review of Literature Journal:American Journal of Medical Genetics, Part A | 2013 | 96 | ||
Maternally inherited leigh syndrome: An unusual cause of infantile apnea Journal:Sleep and Breathing | 2010 | 177 | ||
Successful use of BiPAP in infants with congenital myotonic dystrophy Journal:Pediatrics International | 2013 | 47 |