Mutational analysis of the human MESP1 gene in patients with congenital heart disease reveals a highly variable sequence in exon 1.
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PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger SyndromeTetralogy of Fallot and Hypoplastic Left Heart Syndrome - Complex Clinical Phenotypes Meet Complex Genetic NetworksMESP1 Mutations in Patients with Congenital Heart Defects.Earlier and broader roles of Mesp1 in cardiovascular development.A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease.A novel NKX2.6 mutation associated with congenital ventricular septal defect.
P2860
Mutational analysis of the human MESP1 gene in patients with congenital heart disease reveals a highly variable sequence in exon 1.
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2013 nî lūn-bûn
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Mutational analysis of the hum ...... y variable sequence in exon 1.
@en
Mutational analysis of the hum ...... y variable sequence in exon 1.
@nl
type
label
Mutational analysis of the hum ...... y variable sequence in exon 1.
@en
Mutational analysis of the hum ...... y variable sequence in exon 1.
@nl
prefLabel
Mutational analysis of the hum ...... y variable sequence in exon 1.
@en
Mutational analysis of the hum ...... y variable sequence in exon 1.
@nl
P2093
P1476
Mutational analysis of the hum ...... y variable sequence in exon 1.
@en
P2093
Astrid Werner
Christian Schreiber
Harald Lahm
Johannes Böhm
Julie Cleuziou
Jürgen Hörer
Marcus-André Deutsch
Markus Krane
Martina Dreßen
Rüdiger Lange
P304
P356
10.1016/J.EJMG.2013.09.001
P577
2013-09-19T00:00:00Z