Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statementFrédéric Brioude, Eamonn R. Maher, Jennifer M. Kalish et al.|Nature Reviews Endocrinology|2018Cited by 596
Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndromeChristine Gicquel, Yves Le Bouc, Sylvie Rossignol et al.|Nature Genetics|2005Cited by 504
Diagnosis and management of Silver–Russell syndrome: first international consensus statementEmma Wakeling, Irène Netchine|Nature Reviews Endocrinology|2016Cited by 502
Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiencyIrène Netchine, Serge Amselem, Marie‐Laure Sobrier et al.|Nature Genetics|2000Cited by 366
Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International PerspectivePaulo Ferrez Collett‐Solberg, Joachim Woelfle, Vaman Khadilkar et al.|Hormone Research in Paediatrics|2019Cited by 345