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Publications by Inderjeet Dokal
Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
American Journal of Human Genetics
Genetics
Aberrant 3' Oligoadenylation of Spliceosomal U6 Small Nuclear RNA in Poikiloderma With Neutropenia
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Clinical Utility Gene Card For: Dyskeratosis Congenita – Update 2015
European Journal of Human Genetics
Genetics
A Human Ortholog of Archaeal DNA Repair Protein Hef Is Defective in Fanconi Anemia Complementation Group M
Nature Genetics
Genetics
Telomerase Reverse-Transcriptase Homozygous Mutations in Autosomal Recessive Dyskeratosis Congenita and Hoyeraal-Hreidarsson Syndrome
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Targeted Disruption of Dkc1, the Gene Mutated in X-Linked Dyskeratosis Congenita, Causes Embryonic Lethality in Mice
Oncogene
Cancer Research
Genetics
Molecular Biology
Advances in the Understanding of Dyskeratosis Congenita
British Journal of Haematology
Hematology