A de novo 11p13 Microduplication in a Patient with Some Features Invoking Silver-Russell Syndrome

By  

Molecular Syndromology, Vol. 5, Iss. 1, 2013-11 ,pp. : 11-18

Karger

Access to resources Recommend Favorite

Familial 1.3-Mb 11p15.5p15.4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann Syndromes

By  

Molecular Syndromology, Vol. 6, Iss. 3, 2015-07 ,pp. : 147-151

Karger

Access to resources Recommend Favorite

Paternal duplication of the 11p15 centromeric imprinting control region is associated with increased expression of CDKN1C in a child with Russell–Silver syndrome

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 12, 2015-12 ,pp. : 3229-3233

John Wiley & Sons Inc

Access to resources Recommend Favorite

Haploinsufficiency of ANKRD11 (16q24.3) Is Not Obligatorily Associated with Cognitive Impairment but Shows a Clinical Overlap with Silver-Russell Syndrome

By  

Molecular Syndromology, Vol. 4, Iss. 5, 2013-06 ,pp. : 246-249

Karger

Access to resources Recommend Favorite

Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith–Wiedemann syndrome and Silver–Russell syndrome

By Nativio Raffaella   Sparago Angela   Ito Yoko   Weksberg Rosanna   Riccio Andrea   Murrell Adele  

Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1363-1374

Oxford University Press

Access to resources Recommend Favorite