Growth hormone, gender and face shape in prader–willi syndrome
暂无分享,去创建一个
P. Hammond | M. Suttie | A. Holland | C. McAllister | F. Faravelli | T. Mattina | F. Forzano | M. A. de Souza | C. Perrotta
[1] J. Milašin,et al. Ontogenetic changes of craniofacial complex in Turner syndrome patients treated with growth hormone , 2013, Clinical Oral Investigations.
[2] Peter Hammond,et al. Facial Dysmorphism Across the Fetal Alcohol Spectrum , 2013, Pediatrics.
[3] P. Hammond,et al. Craniofacial characteristics of fragile X syndrome in mouse and man , 2012, European Journal of Human Genetics.
[4] R. Hennekam,et al. The complex craniofacial signature of fibrodysplasia ossificans progressiva: Whose handwriting is it? , 2012 .
[5] Peter Hammond,et al. Atypical face shape and genomic structural variants in epilepsy , 2012, Brain : a journal of neurology.
[6] G. Johnson,et al. Ethanol-Induced Face-Brain Dysmorphology Patterns Are Correlative and Exposure-Stage Dependent , 2012, PloS one.
[7] Peter Hammond,et al. The face signature of fibrodysplasia ossificans progressiva , 2012, American journal of medical genetics. Part A.
[8] R. Hennekam,et al. Another cause of vaccine encephalopathy: a case of Angelman syndrome. , 2012, European journal of medical genetics.
[9] P. Hammond,et al. Large‐scale objective phenotyping of 3D facial morphology , 2012, Human mutation.
[10] C. Savage,et al. The neuroanatomy of genetic subtype differences in Prader–Willi syndrome , 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[11] D. Vandermeulen,et al. Dysmorphometrics: the modelling of morphological abnormalities , 2012, Theoretical Biology and Medical Modelling.
[12] D. J. Driscoll,et al. Unique and atypical deletions in Prader–Willi syndrome reveal distinct phenotypes , 2011, European Journal of Human Genetics.
[13] Rolf P Wurtz,et al. Automated syndrome detection in a set of clinical facial photographs , 2011, American journal of medical genetics. Part A.
[14] R. Hennekam,et al. Uncovering Genomic Causes of Co-Morbidity in Epilepsy: Gene-Driven Phenotypic Characterization of Rare Microdeletions , 2011, PloS one.
[15] Peter Hammond,et al. Fine-grained facial phenotype–genotype analysis in Wolf–Hirschhorn syndrome , 2011, European Journal of Human Genetics.
[16] J. Eickhoff,et al. Long-term growth hormone therapy changes the natural history of body composition and motor function in children with prader-willi syndrome. , 2010, The Journal of clinical endocrinology and metabolism.
[17] J. Lupski,et al. Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet–Biedl syndrome , 2008, Proceedings of the National Academy of Sciences.
[18] P Hammond,et al. Face–brain asymmetry in autism spectrum disorders , 2008, Molecular Psychiatry.
[19] Peter Hammond,et al. The use of 3D face shape modelling in dysmorphology , 2007, Archives of Disease in Childhood.
[20] Tim Hutton,et al. Reproducibility of soft tissue landmarks on three-dimensional facial scans. , 2006, European journal of orthodontics.
[21] A. Karmiloff-Smith,et al. Discriminating power of localized three-dimensional facial morphology. , 2005, American journal of human genetics.
[22] Peter Hammond,et al. GTF2IRD1 in Craniofacial Development of Humans and Mice , 2005, Science.
[23] D. J. Driscoll,et al. Prader-Willi syndrome. , 1984, Current problems in pediatrics.
[24] R. Hennekam,et al. 3D analysis of facial morphology , 2004, American journal of medical genetics. Part A.
[25] Anthony P. Goldstone,et al. Prader-Willi syndrome: advances in genetics, pathophysiology and treatment , 2004, Trends in Endocrinology & Metabolism.
[26] A. Holland,et al. Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome. , 2004, Journal of intellectual disability research : JIDR.
[27] Peter Hammond,et al. Estimating average growth trajectories in shape-space using kernel smoothing , 2003, IEEE Transactions on Medical Imaging.
[28] David Haig,et al. Prader‐Willi syndrome and the evolution of human childhood , 2003, American journal of human biology : the official journal of the Human Biology Council.
[29] A. Holland,et al. Behavioural phenotypes associated with specific genetic disorders: evidence from a population-based study of people with Prader-Willi syndrome , 2002, Psychological Medicine.
[30] A. Holland,et al. Relationship between clinical and genetic diagnosis of Prader-Willi syndrome , 2002, Journal of medical genetics.
[31] A. Holland,et al. Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region. , 2001, Journal of medical genetics.
[32] Emden R. Gansner,et al. Graphviz - Open Source Graph Drawing Tools , 2001, GD.
[33] W. Proffit,et al. The effect of growth hormone on craniofacial growth and dental maturation in Turner syndrome. , 2001, The Angle orthodontist.
[34] M. Butler,et al. Photoanthropometric study of craniofacial traits in individuals with Prader‐Willi syndrome on short‐term growth hormone therapy , 1998, Clinical genetics.
[35] S. Schwartz,et al. Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15. , 1997, American journal of medical genetics.
[36] M. Butler,et al. Photoanthropometric study of craniofacial traits of individuals with Prader-Willi syndrome. , 1995, American journal of medical genetics.
[37] S. Cassidy,et al. Cephalometric analysis of the Prader-Willi syndrome. , 1990, American journal of medical genetics.
[38] M. Butler,et al. Craniofacial variation and growth in the Prader-Labhart-Willi syndrome. , 1987, American journal of physical anthropology.
[39] J. Tanner,et al. EXPERIENCE WITH HUMAN GROWTH HORMONE IN GREAT BRITAIN: THE REPORT OF THE MRC WORKING PARTY , 1979, Clinical endocrinology.
[40] J. Job. Results of long-term growth hormone replacement therapy in children: when and how to treat? , 1990, Hormone research.