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Showing 1 - 2 results of 2 for search 'Romanelli V.', query time: 0.01s Refine Results
1
A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases
A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases
by Kantaputra P.N., Sittiwangkul R., Sonsuwan N., Romanelli V., Tenorio J., Lapunzina P.
Published 2014
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2
A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases
A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases
by Kantaputra P.N., Sittiwangkul R., Sonsuwan N., Romanelli V., Tenorio J., Lapunzina P.
Published 2014
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