| The clinical geneticist and the evaluation of failure to thrive versus failure to feed |
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| What every clinical geneticist should know about testing for osteogenesis imperfecta in suspected child abuse cases |
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| Beyond osteogenesis imperfecta: Causes of fractures during infancy and childhood |
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| Genetic differentials of child abuse: Is your case rare or real? |
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| Common skin and bleeding disorders that can potentially masquerade as child abuse |
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| Epigenetics and child abuse: Modern‐day darwinism — The miraculous ability of the human genome to adapt, and then adapt again |
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| Clinical perspectives on osteogenesis imperfecta versus non‐accidental injury |
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| Recognition and prevention of child abuse in the child with disability |
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| Genetic drift: A case of abuse |
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| Ehlers–Danlos syndrome(s) mimicking child abuse: Is there an impact on clinical practice? |
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| Making chromosome abnormalities treatable conditions |
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| Jacobsen syndrome: Advances in our knowledge of phenotype and genotype |
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| A review of 18p deletions |
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| 5p deletions: Current knowledge and future directions |
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| Consequences of chromsome18q deletions |
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| Wolf–Hirschhorn syndrome: A review and update |
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| Children with Williams syndrome: Developmental trajectories for intellectual abilities, vocabulary abilities, and adaptive behavior |
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| Contrasting age related changes in autism spectrum disorder phenomenology in Cornelia de Lange, Fragile X, and Cri du Chat syndromes: Results from a 2.5 year follow‐up |
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| Down syndrome: Cognitive and behavioral functioning across the lifespan |
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| Developmental trajectories in 22q11.2 deletion syndrome |
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| The developmental trajectory of disruptive behavior in Down syndrome, fragile X syndrome, Prader–Willi syndrome and Williams syndrome |
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| Developmental trajectories as autism phenotypes |
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| Developmental trajectories in cognitive‐behavioral phenotypes: Introduction |
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| Positive effects of early androgen therapy on the behavioral phenotype of boys with 47,XXY |
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| Knowledge, assessment, and management of adults with joint hypermobility syndrome/Ehlers–Danlos syndrome hypermobility type among flemish physiotherapists |
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| <b>Phenotypic variability in developmental coordination disorder:</b> Clustering of generalized joint hypermobility with attention deficit/hyperactivity disorder, atypical swallowing and narrative dif |
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| The neuromuscular differential diagnosis of joint hypermobility |
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| The role of narrative medicine in the management of joint hypermobility syndrome/Ehlers–Danlos syndrome, hypermobility type |
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| Differential diagnosis and diagnostic flow chart of joint hypermobility syndrome/ehlers‐danlos syndrome hypermobility type compared to other heritable connective tissue disorders |
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| Gastrointestinal and nutritional issues in joint hypermobility syndrome/ehlers–danlos syndrome, hypermobility type |
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| <b>Psychopathological manifestations of joint hypermobility and joint hypermobility syndrome/ Ehlers–Danlos syndrome, hypermobility type:</b> The link between connective tissue and psychological distr |
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| Generalized joint hypermobility, joint hypermobility syndrome and Ehlers‐Danlos syndrome, hypermobility type |
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| Neurodevelopmental attributes of joint hypermobility syndrome/Ehlers–Danlos syndrome, hypermobility type: Update and perspectives |
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| Spectrum of mucocutaneous manifestations in 277 patients with joint hypermobility syndrome/Ehlers‐Danlos syndrome, hypermobility type |
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| Connective tissue, Ehlers–Danlos syndrome(s), and head and cervical pain |
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