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Journal Article
Clinical genetics, ISSN 0009-9163, 08/2003, Volume 64, Issue 2, pp. 83 - 95
Rubinstein–Taybi syndrome | thalassemia | Coffin–Lowry syndrome | Rett syndrome | X-linked | chromatin remodeling | histone postranslational modifications | immunodeficiency–centromeric instability–facial anomalies syndrome | chromatin | mental retardation syndrome | α‐thalassemia | Coffin–Lowry syndrome | X‐linked | Rubinstein–Taybi syndrome | immunodeficiency–centromeric instability–facial anomalies syndrome | Centromeric instability-facial anomalies syndrome | Chromatin | Histone postranslational modifications | α-thalassemia/mental retardation syndrome, X-linked | Immunodeficiency | Rubinstein | Coffin-Lowry syndrome | Chromatin remodeling | Taybi syndrome | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Biological and medical sciences | Complex syndromes | Medical sciences | Medical genetics | Coffin-Lowry Syndrome - genetics | Rett Syndrome - complications | alpha-Thalassemia - complications | Mental Retardation, X-Linked - complications | Rett Syndrome - diagnosis | Humans | Genetic Diseases, Inborn - genetics | Chromatin Assembly and Disassembly - genetics | Coffin-Lowry Syndrome - complications | Mutation - genetics | Rubinstein-Taybi Syndrome - complications | Mutation - physiology | Mental Retardation, X-Linked - genetics | Rubinstein-Taybi Syndrome - diagnosis | Rubinstein-Taybi Syndrome - genetics | Mental Retardation, X-Linked - diagnosis | Genetic Diseases, Inborn - complications | alpha-Thalassemia - diagnosis | alpha-Thalassemia - genetics | Rett Syndrome - genetics | Genetic Diseases, Inborn - diagnosis | Chromatin Assembly and Disassembly - physiology | Coffin-Lowry Syndrome - diagnosis | Index Medicus
Journal Article