Related references
Note: Only part of the references are listed.Skeletal Characteristics of WNT1 Osteoporosis in Children and Young Adults
Riikka E. Makitie et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2016)
Osteogenesis imperfecta in children and adolescents-new developments in diagnosis and treatment
P. Trejo et al.
OSTEOPOROSIS INTERNATIONAL (2016)
Mutations in patients with osteogenesis imperfecta from consanguineous Indian families
Joshi Stephen et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2015)
New Genetic Forms of Childhood-Onset Primary Osteoporosis
Anders J. Kampe et al.
HORMONE RESEARCH IN PAEDIATRICS (2015)
Skeletal characteristics associated with homozygous and heterozygous WNT1 mutations
Telma Palomo et al.
BONE (2014)
WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta
Shawna M. Pyott et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Mutations in WNT1 Cause Different Forms of Bone Fragility
Katharina Keupp et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Mutations in WNT1 are a cause of osteogenesis imperfecta
Somayyeh Fahiminiya et al.
JOURNAL OF MEDICAL GENETICS (2013)
WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype
Eissa Faqeih et al.
JOURNAL OF MEDICAL GENETICS (2013)
WNT1 Mutations in Early-Onset Osteoporosis and Osteogenesis Imperfecta
Christine M. Laine et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review
Luis Fernandez et al.
BMC MEDICAL GENETICS (2009)
Zebrafish prickle, a modulator of noncanonical Wnt/Fz signaling, regulates gastrulation movements
MT Veeman et al.
CURRENT BIOLOGY (2003)