Literature DB >> 17097025

PHOX2B mutations in three Chinese patients with congenital central hypoventilation syndrome.

Siu-Fong June Or1, Ming-for Tony Tong, Fai-Man Ivan Lo, Chi-Wai Law, Ting-Yat Miu, Delphine Trochet, Tak-Sum Stephen Lam.   

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Year:  2006        PMID： 17097025

Source DB:  PubMed          Journal:  Chin Med J (Engl)        ISSN： 0366-6999            Impact factor:   2.628


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  2 in total

1.  Cerebral MRI abnormalities in a premature infant with later confirmed congenital central hypoventilation syndrome.

Authors:  Eveline van Delft; Peter Andriessen; Colleen N A L Vaessens; Jan Buijs; Sidarto Bambang Oetomo
Journal:  Eur J Pediatr       Date:  2009-12-02       Impact factor: 3.183

2.  A case of congenital central hypoventilation syndrome with PHOX2B gene mutation in a Korean neonate.

Authors:  Kyoung-Ah Kwon; Su-Eun Park; Shin-Yun Byun; Shine-Young Kim; Sang-Hyoun Hwang
Journal:  J Korean Med Sci       Date:  2010-07-20       Impact factor: 2.153
  2 in total

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