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
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II - ScienceDirect
Primordial Dwarfism: A Case Series From North East of Iran and Literature Review - Journal of Pediatrics Review
Genetics for the pediatric endocrinologists – 2 Primordial short stature in children and adolescents - Journal of Pediatric Endocrinology and Diabetes
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with lissencephaly and brain cyst - ScienceDirect
IJMS | Free Full-Text | Whole-Exome and Transcriptome Sequencing Expands the Genotype of Majewski Osteodysplastic Primordial Dwarfism Type II
A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II) | Semantic Scholar
Mutations in the Pericentrin (PCNT) Gene Cause Primordial Dwarfism | Science
Effect of recombinant insulin-like growth factor-1 treatment on short-term linear growth in a child with Majewski osteodysplastic primordial dwarfism type II and hepatic insufficiency
Rational Design of Potent Peptide Inhibitors of the PD-1:PD-L1 Interaction for Cancer Immunotherapy | Journal of the American Chemical Society
Identification of RNU4ATAC mutations in MOPD I patients. (A)... | Download Scientific Diagram
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
Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene. - Abstract - Europe PMC
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
Frontiers | A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II)
Microcephalic osteodysplastic primordial dwarfism type 1 | BMJ Case Reports
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with lissencephaly and brain cyst - ScienceDirect
Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene. - Abstract - Europe PMC
Primordial Dwarfism: Life Expectancy, Pictures, Symptoms, Types, More
Microcephalic osteodysplastic primordial dwarfism type 1 | BMJ Case Reports
Frontiers | A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II)
Binding activity of the 15.5K protein to the 5 ′ stem–loop of MOPD I... | Download Scientific Diagram
Mutations in U4atac snRNA, a Component of the Minor Spliceosome, in the Developmental Disorder MOPD I | Science
