Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with lissencephaly and brain cyst - ScienceDirect
Binding activity of the 15.5K protein to the 5 ′ stem–loop of MOPD I... | Download Scientific Diagram
A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder - Abdel‐Salam - 2011 - American Journal of Medical Genetics Part
Primordial Dwarfism: A Case Series From North East of Iran and Literature Review - Journal of Pediatrics Review
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II - ScienceDirect
PDF) Striking Hematological Abnormalities in Patients With Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II): A Potential Role of Pericentrin in Hematopoiesis
A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder - Abdel‐Salam - 2011 - American Journal of Medical Genetics Part
A novel homozygous mutation of the PCNT gene in a Chinese patient with microcephalic osteodysplastic primordial dwarfism type II - Liu - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Identification of RNU4ATAC mutations in MOPD I patients. (A)... | Download Scientific Diagram
A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder - Abdel‐Salam - 2011 - American Journal of Medical Genetics Part
Genes | Free Full-Text | Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ
Case Report Clinical Findings and Dental Manifestations Associated With Microcephalic Osteodysplastic Primordial Dwarfism Type I
Frontiers | A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II)
Phenotypic traits of patients with microcephalic osteodysplastic... | Download Scientific Diagram
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II - ScienceDirect
Microcephalic osteodysplastic primordial dwarfism type 1 | BMJ Case Reports
Genetics for the pediatric endocrinologists – 2 Primordial short stature in children and adolescents - Journal of Pediatric Endocrinology and Diabetes
Mutations in U4atac snRNA, a Component of the Minor Spliceosome, in the Developmental Disorder MOPD I | Science
Mutations in the Pericentrin (PCNT) Gene Cause Primordial Dwarfism | Science
Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene. - Abstract - Europe PMC
Primordial Dwarfism: Life Expectancy, Pictures, Symptoms, Types, More
A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II) | Semantic Scholar
Rational Design of Potent Peptide Inhibitors of the PD-1:PD-L1 Interaction for Cancer Immunotherapy | Journal of the American Chemical Society
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II - ScienceDirect
A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder - Abdel‐Salam - 2011 - American Journal of Medical Genetics Part
Majewski osteodysplastic primordial dwarfism type II (MOPD II): Natural history and clinical findings - Hall - 2004 - American Journal of Medical Genetics Part A - Wiley Online Library
