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
Microcephalic osteodysplastic primordial dwarfism type II: MedlinePlus Genetics
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
Figure 1 from Majewski osteodysplastic primordial dwarfism type II: clinical findings and dental management of a child patient | Semantic Scholar
Characteristic features of MOPDII. a Patient 1. A 7-week-old female... | 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
Rational Design of Potent Peptide Inhibitors of the PD-1:PD-L1 Interaction for Cancer Immunotherapy | Journal of the American Chemical Society
Genetics for the pediatric endocrinologists – 2 Primordial short stature in children and adolescents - Journal of Pediatric Endocrinology and Diabetes
Microcephalic Osteodysplastic Primordial Dwarfism Type I/III
Binding activity of the 15.5K protein to the 5 ′ stem–loop of MOPD I... | Download Scientific Diagram
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
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
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
Identification of RNU4ATAC mutations in MOPD I patients. (A)... | Download Scientific Diagram
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II - ScienceDirect
Frontiers | A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II)
Mutations in the Pericentrin (PCNT) Gene Cause Primordial Dwarfism | Science
Rational Design of Potent Peptide Inhibitors of the PD-1:PD-L1 Interaction for Cancer Immunotherapy | Journal of the American Chemical Society
Mutations in U4atac snRNA, a Component of the Minor Spliceosome, in the Developmental Disorder MOPD I | Science
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II - ScienceDirect
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II | Semantic Scholar
