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Publications by Amanda J. Walne
Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
American Journal of Human Genetics
Genetics
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Mutations in the Telomerase Component NHP2 Cause the Premature Ageing Syndrome Dyskeratosis Congenita
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A Vietnamese Case of Dyskeratosis Congenita
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Telomerase Reverse-Transcriptase Homozygous Mutations in Autosomal Recessive Dyskeratosis Congenita and Hoyeraal-Hreidarsson Syndrome
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Bilateral Proliferative Retinopathy Associated With Hoyeraal-Hreidarsson Syndrome, a Severe Form of Dyskeratosis Congenita
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Outcome of Haematopoietic Stem Cell Transplantation in Dyskeratosis Congenita
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The Diagnosis and Treatment of Dyskeratosis Congenita: A Review
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Clinical Utility Gene Card For: Dyskeratosis Congenita – Update 2015
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Dyskeratosis Congenita: Three Additional Families Show Linkage to a Locus in Xq28.
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