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

[1]  T. Spector,et al.  The Three-Factor Eating Questionnaire, body mass index, and responses to sweet and salty fatty foods: a twin study of genetic and environmental associations. , 2008, The American journal of clinical nutrition.

[2]  K. Rauen,et al.  Interstitial deletions of chromosome 6q: genotype–phenotype correlation utilizing array CGH , 2007, Clinical genetics.

[3]  Reinhard Ullmann,et al.  Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome. , 2007, American journal of human genetics.

[4]  C. Kim,et al.  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. , 2006, European journal of medical genetics.

[5]  C. Kim,et al.  A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity. , 2006, European journal of medical genetics.

[6]  J. Vermeesch,et al.  Interstitial 6q deletion: clinical and array CGH characterisation of a new patient. , 2005, European journal of medical genetics.

[7]  P. Beales,et al.  Lifting the lid on Pandora's box: the Bardet-Biedl syndrome. , 2005, Current opinion in genetics & development.

[8]  Dai Zhang,et al.  Family‐based association study between autism and glutamate receptor 6 gene in Chinese Han trios , 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[9]  K. Devriendt,et al.  Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders , 2004, European Journal of Human Genetics.

[10]  E. Haan,et al.  Birth prevalence of Prader-Willi syndrome in Australia , 2003, Archives of disease in childhood.

[11]  R. Zori,et al.  Concurrence of fragile X syndrome and 47, XYY in an individual with a Prader‐Willi‐like phenotype , 2003, American journal of medical genetics. Part A.

[12]  A. Munnich,et al.  Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype , 2002, Journal of medical genetics.

[13]  T. Bourgeron,et al.  Linkage and association of the glutamate receptor 6 gene with autism , 2002, Molecular Psychiatry.

[14]  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.

[15]  Christopher P. Austin,et al.  Identification and characterization of a second melanin-concentrating hormone receptor, MCH-2R , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[16]  H. Arnold,et al.  Isolation and characterization of the novel popeye gene family expressed in skeletal muscle and heart. , 2000, Developmental biology.

[17]  F. Gabreëls,et al.  Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature. , 2000, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

[18]  A. Zinn,et al.  Profound obesity associated with a balanced translocation that disrupts the SIM1 gene. , 2000, Human molecular genetics.

[19]  G. Feldman,et al.  Prader-Willi-like syndrome in a patient with an Xq23q25 duplication. , 1998, American journal of medical genetics.

[20]  J. Hoo,et al.  Interstitial 6q deletion and Prader‐Willi‐like phenotype , 1996, Clinical genetics.

[21]  M. Urioste,et al.  De novo interstitial deletion q16.2q21 on chromosome 6. , 1995, American journal of medical genetics.

[22]  B. D. de Vries,et al.  The Prader-Willi-like phenotype in fragile X patients: a designation facilitating clinical (and molecular) differential diagnosis. , 1994, Journal of medical genetics.

[23]  R. Huganir,et al.  Human GluR6 kainate receptor (GRIK2): molecular cloning, expression, polymorphism, and chromosomal assignment. , 1994, Genomics.

[24]  M. Cabanis,et al.  6q1 monosomy: a distinctive syndrome , 1988, Clinical genetics.