Detailed phenotype–genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader–Willi-like phenotype

References

Page 1

	Year	Citations
Profound obesity associated with a balanced translocation that disrupts the SIM1 gene J. L. Human Molecular Genetics	2000	396
Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome Eva Klopocki, Harald Schulze, Gabriele Strauß, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsHematologyClinical Genetics	2007	367
Linkage and association of the glutamate receptor 6 gene with autism Stéphane Jamain, Catalina Betancur, Hélène Quach, Molecular Psychiatry Glutamate Receptor 6Syndromic AutismGeneticsPsychiatric GeneticsAutism	2002	304
Identification and characterization of a second melanin-concentrating hormone receptor, MCH-2R Andreas W. Sailer, Hideki Sano, Zhizhen Zeng, Proceedings of the National Academy of Sciences	2001	239
The Three-Factor Eating Questionnaire, body mass index, and responses to sweet and salty fatty foods: a twin study of genetic and environmental associations Kaisu Keskitalo, Hely Tuorila, Tim D. Spector, American Journal of Clinical Nutrition Food ChoiceObesityNutritionNutritional EpidemiologyBody Mass Index	2008	218
Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders Annick Vogels, Jenneke van den Ende, Kathelijn Keymolen, European Journal of Human Genetics Clinical EpidemiologyPediatricsPrader–willi SyndromePublic HealthBirth Incidence	2003	184
Isolation and Characterization of the Novel Popeye Gene Family Expressed in Skeletal Muscle and Heart Birgit Andrée, Tina Hillemann, Gania Kessler‐Icekson, Developmental Biology Cardiac MuscleCardiomyopathyFunctional GenomicsMolecular PhysiologySkeletal Muscle	2000	131
Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems Carla S. D’Angelo, José Albino da Paz, Chong Ae Kim, European Journal of Medical Genetics PsychiatryGenetic DisorderMedicineBehavioral ProblemsNeuropsychiatry	2006	122
Birth prevalence of Prader-Willi syndrome in Australia Arabella Smith Archives of Disease in Childhood	2003	118
Family‐based association study between autism and glutamate receptor 6 gene in Chinese Han trios Shuang Mei, Jing Liu, Mei Xiang Jia, American Journal of Medical Genetics Part B Neuropsychiatric Genetics Glutamate Receptor 6Chinese Han TriosSyndromic AutismGeneticsPsychiatric Genetics	2004	103

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