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Publications by Betül Kılıç
Novel Mutation and Severe Respiratory Failure in Congenital Disorders of Glycosylation Type Ix
Turkish Journal of Pediatrics
Child Health
Pediatrics
Perinatology
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Congenital Disorders of Glycosylation. Part I. Defects of Protein N-Glycosylation.
Acta Biochimica Polonica
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Fibrotic Response in Fibroblasts From Congenital Disorders of Glycosylation
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MPDU1 Mutations Underlie a Novel Human Congenital Disorder of Glycosylation, Designated Type If
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Novel Compound Heterozygous COG5 Mutations in a Chinese Male Patient With Severe Clinical Symptoms and Type�IIi Congenital Disorder of Glycosylation: A Case Report
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Modeling Congenital Disorders of N-Linked Glycoprotein Glycosylation in Drosophila Melanogaster
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The Congenital Disorders of Glycosylation: A Multifaceted Group of Syndromes
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Novel NKX2.1 Mutation Associated With Hypothyroidism and Lethal Respiratory Failure in a Full-Term Neonate
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