File Download
 
 
Supplementary

Conference Paper: Differential liabilities of rare coding and common non-coding RET mutations explain the multifactorial genetics of Hirschsprung disease.
  • Basic View
  • Metadata View
  • XML View
TitleDifferential liabilities of rare coding and common non-coding RET mutations explain the multifactorial genetics of Hirschsprung disease.
 
AuthorsEmison, E
Burzynski, G
Amiel, J
Borrego, S
Ceccherini,, I
Fernandez, R
Garcia-Barcelo, MM
Griseri, P
Hofstra, R
Kashuk, CS
Lantieri, F
Lyonnet, S
Tam, PKH
Pecina, A
Tullio-Pelet,, A
West, K
Chakravarti, A
 
Issue Date2005
 
DC FieldValue
dc.contributor.authorEmison, E
 
dc.contributor.authorBurzynski, G
 
dc.contributor.authorAmiel, J
 
dc.contributor.authorBorrego, S
 
dc.contributor.authorCeccherini,, I
 
dc.contributor.authorFernandez, R
 
dc.contributor.authorGarcia-Barcelo, MM
 
dc.contributor.authorGriseri, P
 
dc.contributor.authorHofstra, R
 
dc.contributor.authorKashuk, CS
 
dc.contributor.authorLantieri, F
 
dc.contributor.authorLyonnet, S
 
dc.contributor.authorTam, PKH
 
dc.contributor.authorPecina, A
 
dc.contributor.authorTullio-Pelet,, A
 
dc.contributor.authorWest, K
 
dc.contributor.authorChakravarti, A
 
dc.date.accessioned2010-09-26T00:47:43Z
 
dc.date.available2010-09-26T00:47:43Z
 
dc.date.issued2005
 
dc.identifier.hkuros103890
 
dc.identifier.urihttp://hdl.handle.net/10722/108631
 
dc.languageeng
 
dc.relation.ispartofGordon Research Conference on Human Genetics and Genomics Salve Regina University Newport, RI, USA, July 24-29, 2005
 
dc.titleDifferential liabilities of rare coding and common non-coding RET mutations explain the multifactorial genetics of Hirschsprung disease.
 
dc.typeConference_Paper
 
<?xml encoding="utf-8" version="1.0"?>
<item><contributor.author>Emison, E</contributor.author>
<contributor.author>Burzynski, G</contributor.author>
<contributor.author>Amiel, J</contributor.author>
<contributor.author>Borrego, S</contributor.author>
<contributor.author>Ceccherini,, I</contributor.author>
<contributor.author>Fernandez, R</contributor.author>
<contributor.author>Garcia-Barcelo, MM</contributor.author>
<contributor.author>Griseri, P</contributor.author>
<contributor.author>Hofstra, R</contributor.author>
<contributor.author>Kashuk, CS</contributor.author>
<contributor.author>Lantieri, F</contributor.author>
<contributor.author>Lyonnet, S</contributor.author>
<contributor.author>Tam, PKH</contributor.author>
<contributor.author>Pecina, A</contributor.author>
<contributor.author>Tullio-Pelet,, A</contributor.author>
<contributor.author>West, K</contributor.author>
<contributor.author>Chakravarti, A</contributor.author>
<date.accessioned>2010-09-26T00:47:43Z</date.accessioned>
<date.available>2010-09-26T00:47:43Z</date.available>
<date.issued>2005</date.issued>
<identifier.uri>http://hdl.handle.net/10722/108631</identifier.uri>
<language>eng</language>
<relation.ispartof>Gordon Research Conference on Human Genetics and Genomics  Salve Regina University Newport, RI, USA, July 24-29, 2005</relation.ispartof>
<title>Differential liabilities of rare coding and common non-coding RET mutations explain the multifactorial genetics of Hirschsprung disease.</title>
<type>Conference_Paper</type>
<identifier.hkuros>103890</identifier.hkuros>
</item>