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15653965
Source:
http://linkedlifedata.com/resource/pubmed/id/15653965
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pubmed-article:15653965
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pubmed-article:15653965
pubmed:issue
1
lld:pubmed
pubmed-article:15653965
pubmed:dateCreated
2005-1-17
lld:pubmed
pubmed-article:15653965
pubmed:abstractText
To analyze the main clinical features, genetic mutations, and outcomes of patients of the French Congenital Central Hypoventilation Syndrome (CCHS) Registry.
lld:pubmed
pubmed-article:15653965
pubmed:language
eng
lld:pubmed
pubmed-article:15653965
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http://linkedlifedata.com/r...
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AIM
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MEDLINE
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pubmed-article:15653965
pubmed:month
Jan
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pubmed-article:15653965
pubmed:issn
0012-3692
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pubmed-author:AmielJeanneJ
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pubmed:issnType
Print
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pubmed-article:15653965
pubmed:volume
127
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pubmed-article:15653965
pubmed:owner
NLM
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pubmed-article:15653965
pubmed:authorsComplete
Y
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pubmed-article:15653965
pubmed:pagination
72-9
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pubmed-article:15653965
pubmed:dateRevised
2006-11-15
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pubmed-article:15653965
pubmed:year
2005
lld:pubmed
pubmed-article:15653965
pubmed:articleTitle
The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype.
lld:pubmed
pubmed-article:15653965
pubmed:affiliation
Service de Physiologie, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Université Paris 7, Paris, France. ha.trang@rdb.ap-hop-paris.fr
lld:pubmed
pubmed-article:15653965
pubmed:publicationType
Journal Article
lld:pubmed
pubmed-article:15653965
pubmed:publicationType
Research Support, Non-U.S. Gov't
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