Novel nonsenseGNASmutation in a 14-month-old boy with plate-like osteoma cutis and medulloblastoma

Dissecting the genomic complexity underlying medulloblastoma

(2012) David T. W. Jones et al.   NATURE

Infantile Osteoma Cutis as a Presentation of a GNAS Mutation

(2012) John Martin et al.   PEDIATRIC DERMATOLOGY

Pseudohypoparathyroidism type 1a and the GNAS p.R231H mutation: Somatic mosaicism in a mother with two affected sons

(2010) Ying Fai Ngai et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Osteoma Cutis as the Presenting Feature of Albright Hereditary Osteodystrophy Associated with Pseudopseudohypoparathyroidism

(2010) Ki-Heon Jeong et al.   Annals of Dermatology

Inherited human diseases of heterotopic bone formation

(2010) Eileen M. Shore et al.   Nature Reviews Rheumatology

Congenital Plate-like Osteoma Cutis in an Infant

(2009) ANGELA HERNANDEZ-MARTIN et al.   PEDIATRIC DERMATOLOGY

Diagnostic and mutational spectrum of progressive osseous heteroplasia (POH) and other forms ofGNAS‐based heterotopic ossification

(2008) N.S. Adegbite et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Compound Heterozygous Mutations in theGNASGene of a Boy with Morbid Obesity, Thyroid-Stimulating Hormone Resistance, Pseudohypoparathyroidism, and a Prothrombotic State

(2008) Kathleen Freson et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM