ERBKRANKHEITEN, GENETISCHE KRANKHEITEN (MEDIZIN)

Molecular genetics of inherited eye disorders

0 Type: Book

Epigenetics: current research and emerging trends

by Chadwick, Brian P.

0 Type: Book

Attention, genes, and developmental disorders

by Cornish, Kim, Wilding, John

fromOxford series in developmental cognitive neuroscience

0 Type: Book

Epigenetic biomarkers and diagnostics

fromTranslational epigenetics series

0 Type: Book

Nonsense mutation correction in human diseases: an approach for targeted medicine

by Benhabiles, Hana, Jia, Jieshuang, Lejeune, Fabrice

0 Type: Book

Spinal muscular atrophy: disease mechanisms and therapy

0 Type: Book

Genome stability: from virus to human application

by Kovalchuk, Igor, Kovalchuk, Olga

fromTranslational epigenetics series

0 Type: Book

Medical epigenetics

fromTranslational epigenetics series

0 Type: Book

Gene discovery for disease models

by Gu, Weikuan

0 Type: Book

Atlas of genetic diagnosis and counseling

by Chen, Harold

0 Type: Book

Atlas of genetic diagnosis and counseling

by Chen, Harold

0 Type: Book

Phenotypic variation: exploration and functional genomics

by Smith, Moyra

0 Type: Book

Secondary findings in genomic research

fromTranslational and applied genomics series

0 Type: Book

Mitochondrial disease genes compendium: from genes to clinical manifestations

0 Type: Book

Books

Account

Molecular genetics of inherited eye disorders

Epigenetics: current research and emerging trends

Attention, genes, and developmental disorders

Epigenetic biomarkers and diagnostics

Nonsense mutation correction in human diseases: an approach for targeted medicine

Spinal muscular atrophy: disease mechanisms and therapy

Genome stability: from virus to human application

Medical epigenetics

Gene discovery for disease models

Atlas of genetic diagnosis and counseling

Atlas of genetic diagnosis and counseling

Phenotypic variation: exploration and functional genomics

Secondary findings in genomic research

Mitochondrial disease genes compendium: from genes to clinical manifestations

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