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ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetryNovel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomaliesDNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary DyskinesiaGlobal genetic analysis in mice unveils central role for cilia in congenital heart diseaseTelomeric repeat mutagenicity in human somatic cells is modulated by repeat orientation and G-quadruplex stability.Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis.Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects.Role of cilia in structural birth defects: insights from ciliopathy mutant mouse models.Werner syndrome protein suppresses the formation of large deletions during the replication of human telomeric sequences.Coincident myelomeningocele and gastroschisis: report of 2 cases
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P50
description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Rama Rao Damerla
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Rama Rao Damerla
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Rama Rao Damerla
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Rama Rao Damerla
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Rama Rao Damerla
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type
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Rama Rao Damerla
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Rama Rao Damerla
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Rama Rao Damerla
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Rama Rao Damerla
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Rama Rao Damerla
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Rama Rao Damerla
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Rama Rao Damerla
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Rama Rao Damerla
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Rama Rao Damerla
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Rama Rao Damerla
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P106
P21
P31
P496
0000-0001-6815-0097