Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion

[1] Hopkin RJ(1997)New insights into the phenotypes of 6q deletions Am J Med Genet 70 377-386

[2] Schorry E(2008)Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotype Eur J Hum Genet 16 1443-1449

[3] Bofinger M(2009)Autistic features with speech delay in a girl with an approximately 1.5-Mb deletion in 6q16.1, including GPR63 and FUT9 Clin Genet 75 199-202

[4] Milatovich A(2005)Three cases with de novo 6q imbalance and variable prenatal phenotype Am J Med Genet A 136 254-258

[5] Stern HJ(2007)Interstitial deletion of 6q without phenotypic effect Am J Med Genet A 143 1354-1357

[6] Jayne C(2007)Interstitial deletions of chromosome 6q: karyotype/phenotypecorrelation utilizing array CGH Clin Genet 71 260-266

[7] Bonaglia MC(2005)Interstitial 6q deletion: clinical and array CGH characterisation of a new patient Eur J Med Genet 48 339-345

[8] Ciccone R(2012)Karyotype/phenotypecorrelation in interstitial 6q deletions: a report of 12 new cases Neurogenetics 13 31-47

[9] Gimelli G(2009)Microdeletion of 6q161 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report Mol Cytogenet 7 17-88

[10] Gimelli S(2010)A de novo proximal 6q deletion confirmed by array comparative genomic hybridization Korean J Lab Med 30 84-140

[1] Hopkin RJ(1997)New insights into the phenotypes of 6q deletions Am J Med Genet 70 377-386

[2] Schorry E(2008)Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotype Eur J Hum Genet 16 1443-1449

[3] Bofinger M(2009)Autistic features with speech delay in a girl with an approximately 1.5-Mb deletion in 6q16.1, including GPR63 and FUT9 Clin Genet 75 199-202

[4] Milatovich A(2005)Three cases with de novo 6q imbalance and variable prenatal phenotype Am J Med Genet A 136 254-258

[5] Stern HJ(2007)Interstitial deletion of 6q without phenotypic effect Am J Med Genet A 143 1354-1357

[6] Jayne C(2007)Interstitial deletions of chromosome 6q: karyotype/phenotypecorrelation utilizing array CGH Clin Genet 71 260-266

[7] Bonaglia MC(2005)Interstitial 6q deletion: clinical and array CGH characterisation of a new patient Eur J Med Genet 48 339-345

[8] Ciccone R(2012)Karyotype/phenotypecorrelation in interstitial 6q deletions: a report of 12 new cases Neurogenetics 13 31-47

[9] Gimelli G(2009)Microdeletion of 6q161 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report Mol Cytogenet 7 17-88

[10] Gimelli S(2010)A de novo proximal 6q deletion confirmed by array comparative genomic hybridization Korean J Lab Med 30 84-140