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2009, Annals of the New York Academy of Sciences, ISBN 1573317314, Volume 1151., x, 167
Book
2008, ISBN 0195313763, xiv, 220
Book
2006, Oxford Monographs on Medical Genetics, ISBN 9780195174328, xix, 317
Recent advances in neuroscience and genetics have greatly expanded our understanding of the brain and of the etiological factors involved in developmental... 
genetics | Etiology | Infant | Genetic aspects | Mental retardation | Child | Developmental disabilities | Clinical & internal medicine
Book
Frontiers in Molecular Biosciences, ISSN 2296-889X, 05/2017, Volume 4, Issue MAY, p. 24
Delineation of underlying genomic and genetic factors in a specific disease may be valuable in establishing a definitive diagnosis and may guide patient... 
Rare diseases | Pharmacogenetics | Common diseases | Cancer diagnosis | Nucleic acid sequencing | rare diseases | nucleic acid sequencing | common diseases | cancer diagnosis | BIOCHEMISTRY & MOLECULAR BIOLOGY | pharmacogenetics
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 01/2009, Volume 1151, Issue 1, pp. 1 - 21
The breadth and scope of new information makes difficult a selection of topics to be included in a limited review of highlights of the year. Admittedly, the... 
Duffy antigen | microRNA (miRNA) | pluripotent stem cell | sexual differentiation | human genome | copy number variant or variation (CNV) | HIV-AIDS | schizophrenia | malaria | epigenetics
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 01/2009, Volume 1151, pp. 1 - 21
The breadth and scope of new information makes difficult a selection of topics to be included in a limited review of highlights of the year. Admittedly, the... 
Schizophrenia | Antigens | Malaria | Medical genetics | Stem cells
Journal Article
Annals of the New York Academy of Sciences, 01/2009, Volume 1151, pp. ix - x
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 01/2009, Volume 1151, Issue 1, pp. ix - x
Journal Article
Mitochondrion, ISSN 1567-7249, 05/2019, Volume 46, pp. 262 - 269
Autosomal Dominant Optic Atrophy (ADOA) is a neuro-ophthalmic disease characterized by progressive bilateral vision loss, pallor of the optic disc, central... 
Autosomal dominant | Mitochondria | Optic atrophy | OPA1 | Ataxia | Genotype/phenotype | Meta-analysis | Hearing loss | Myopathy | Genetic research | Disease susceptibility | Genetic aspects | Analysis | Genes
Journal Article
Journal of Alzheimer's Disease, ISSN 1387-2877, 2017, Volume 56, Issue 3, pp. 929 - 938
Journal Article
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