Meier–Gorlin syndrome genotype–phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis

Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome

(2011) Duane L Guernsey et al.   NATURE GENETICS

Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome

(2011) Louise S Bicknell et al.   NATURE GENETICS

Mutations in the pre-replication complex cause Meier-Gorlin syndrome

(2011) Louise S Bicknell et al.   NATURE GENETICS

Elements of morphology: Standard terminology for the ear

(2009) Alasdair Hunter et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Continuous growth reference from 24thweek of gestation to 24 months by gender

(2008) Aimon Niklasson et al.   BMC Pediatrics

Consensus Statement on the Diagnosis and Treatment of Children with Idiopathic Short Stature: A Summary of the Growth Hormone Research Society, the Lawson Wilkins Pediatric Endocrine Society, and the European Society for Paediatric Endocrinology Workshop

(2008) P. Cohen et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM