Showing results 3 to 5 of 5
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| Title | Author(s) | Issue Date | Views | |
|---|---|---|---|---|
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 | 112 | ||
Maternally inherited leigh syndrome: An unusual cause of infantile apnea Journal:Sleep and Breathing | 2010 | 903 | ||
Successful use of BiPAP in infants with congenital myotonic dystrophy Journal:Pediatrics International | 2013 | 39 |