Associated Papers
Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases.
Merello E et al.
European Journal of Medical Genetics, 2013
A systematic review of genetic skeletal disorders reported in Chinese biomedical journals between 1978 and 2012.
Cui Y et al.
Orphanet Journal of Rare Diseases, 2012
A novel HLXB9 mutation in a Chinese family with Currarino syndrome.
Wang Y et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [et Al] = Zeitschrift Fur Kinderchirurgie, 2012
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