CRELD1基因在汉族完全型房室间隔缺损患儿心肌组织表达情况的初步分析(4)
参见附件。
[16]Maslen CL，Babcock D，Robinson SW，et al.CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defect in down syndrome[J].Am J Med Genet A，2006，140(22)：2501-2505.
[17]Zatyka M，Priestley M，Ladusans EJ，et al.Analysis of CRELD1 as a candidate 3p25 atrioventicular septal defect locus (AVSD2)[J].Clin Genet，2005，67(6)：526-528.
[18]Sarkozy A，Esposito G，Conti E，et al.CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects[J].Am J Med Genet A，2005，139(3)：236-238.
[19]Posch MG，Perrot A，Schmitt K，et al.Mutations in GATA4， NKX2.5， CRELD1， and BMP4 are infrequently found in patients with congenital cardiac septal defects [J].Am J Med Genet A，2008，146A(2)：251-253.
[20]Lincoln J， Alfieri CM， Yutzey KE.BMP and FGF regulatory pathways control cell lineage diversification of heart valve precursor cells [J].Dev Biol，2006，292(2)：292-302.
[21]Iwamoto R，Mekada E.ErbB and HB-EGF signaling in heart development and function[J].Cell Struct Funct，2006，31(1)：1-14.
[22]Yoshioka K，Matsuda F，Takakura K，et al.Determination of genes involved in the process of implantation：Application of Gene Chip to scan 6500 genes[J].Biochem Biophys Res，2000，272(2)：531-538.
[23]Patel ZM，Gawde HM，Khatkhatay MI.22q11 microdeletion studies in the heart tissue of an abortus involving a familial form of congenital heart disease[J].J Clin Lab Anal，2006，20(4)：160-163.
[24]Miertus J，Amoroso A.Microarray-based genetics of cardiac malformations[J].Ital Heart J，2001，2(8)：565-567.
[25]Kaynak B，von Heydebreck A，Mebus S.Genome-wide array analysis of normal and malformed human hearts[J].Circulation，2003，107：2467.
[26]Sharma HS，Peters TH，Moorhouse MJ.DNA microarray analysis for human congenital heart disease[J].Cell Biochem Biophys，2006，44(1)：1-9.
[16]Maslen CL，Babcock D，Robinson SW，et al.CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defect in down syndrome[J].Am J Med Genet A，2006，140(22)：2501-2505.
[17]Zatyka M，Priestley M，Ladusans EJ，et al.Analysis of CRELD1 as a candidate 3p25 atrioventicular septal defect locus (AVSD2)[J].Clin Genet，2005，67(6)：526-528.
[18]Sarkozy A，Esposito G，Conti E，et al.CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects[J].Am J Med Genet A，2005，139(3)：236-238.
[19]Posch MG，Perrot A，Schmitt K，et al.Mutations in GATA4， NKX2.5， CRELD1， and BMP4 are infrequently found in patients with congenital cardiac septal defects [J].Am J Med Genet A，2008，146A(2)：251-253.
[20]Lincoln J， Alfieri CM， Yutzey KE.BMP and FGF regulatory pathways control cell lineage diversification of heart valve precursor cells [J].Dev Biol，2006，292(2)：292-302.
[21]Iwamoto R，Mekada E.ErbB and HB-EGF signaling in heart development and function[J].Cell Struct Funct，2006，31(1)：1-14.
[22]Yoshioka K，Matsuda F，Takakura K，et al.Determination of genes involved in the process of implantation：Application of Gene Chip to scan 6500 genes[J].Biochem Biophys Res，2000，272(2)：531-538.
[23]Patel ZM，Gawde HM，Khatkhatay MI.22q11 microdeletion studies in the heart tissue of an abortus involving a familial form of congenital heart disease[J].J Clin Lab Anal，2006，20(4)：160-163.
[24]Miertus J，Amoroso A.Microarray-based genetics of cardiac malformations[J].Ital Heart J，2001，2(8)：565-567.
[25]Kaynak B，von Heydebreck A，Mebus S.Genome-wide array analysis of normal and malformed human hearts[J].Circulation，2003，107：2467.
[26]Sharma HS，Peters TH，Moorhouse MJ.DNA microarray analysis for human congenital heart disease[J].Cell Biochem Biophys，2006，44(1)：1-9.
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