Striking hematological abnormalities in patients with microcephalic osteodysplastic primordial dwarfism type II (MOPD II): A potential role of pericentrin in hematopoiesis

Growth in individuals with Majewski osteodysplastic primordial dwarfism type II caused by pericentrin mutations

(2012) Michael B. Bober et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Fracture Healing of an Osteodysplastic Femur in a Microcephalic Osteodysplastic Primordial Dwarfism II (MOPD II) Patient: A Case Report

(2012) Lisanne Rigter et al.   EUROPEAN JOURNAL OF PEDIATRIC SURGERY

Medical management of moyamoya disease and recurrent stroke in an infant with Majewski osteodysplastic primordial dwarfism type II (MOPD II)

(2012) Esra Kılıç et al.   EUROPEAN JOURNAL OF PEDIATRICS

Cranial Vault Remodeling in Microcephalic Osteodysplastic Primordial Dwarfism Type II and Craniosynostosis

(2012) Michael Engel et al.   JOURNAL OF CRANIOFACIAL SURGERY

Clinical and Functional Characterization of a Patient Carrying a Compound Heterozygous Pericentrin Mutation and a Heterozygous IGF1 Receptor Mutation

(2012) Eva Müller et al.   PLoS One

The smallest teeth in the world are caused by mutations in the PCNT gene

(2011) Piranit Kantaputra et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The shortest of the short: Pericentrin mutations and beyond

(2011) Anita Rauch   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

Moyamoya Disease in Children with Congenital Dwarfing Conditions

(2011) Parham Moftakhar et al.   PEDIATRIC NEUROSURGERY

Microcephalic osteodysplastic dwarfism (Type ll-like) in siblings

(2010) Alain Verloes et al.   CLINICAL GENETICS

Majewski osteodysplastic primordial dwarfism type II (MOPD II) syndrome previously diagnosed as Seckel syndrome: Report of a novel mutation of thePCNTgene

(2009) Maria Piane et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Pericentrin in cellular function and disease

(2009) Benedicte Delaval et al.   JOURNAL OF CELL BIOLOGY

Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families

(2009) M. Willems et al.   JOURNAL OF MEDICAL GENETICS

Multiple intracranial aneurysms and moyamoya disease associated with microcephalic osteodysplastic primordial dwarfism type II: surgical considerations

(2009) James S. Waldron et al.   Journal of Neurosurgery-Pediatrics

Mutations in the Pericentrin (PCNT) Gene Cause Primordial Dwarfism

(2008) A. Rauch et al.   SCIENCE